Neurostimulation titration process

- LivaNova USA, Inc.

Systems and methods are provided for delivering neurostimulation therapies to patients for treating chronic heart failure. A titration process is used to gradually increase the stimulation intensity to a desired therapeutic level. This titration process can minimize the amount of time required to complete titration so as to begin delivery of the stimulation at therapeutically desirable levels.

Skip to: Description  ·  Claims  ·  References Cited  · Patent History  ·  Patent History
Description
CROSS-REFERENCE TO RELATED PATENT APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 14/457,807, filed Aug. 12, 2014, now U.S. Pat. No. 9,533,153, which is incorporated herein by reference in its entirety.

BACKGROUND

Chronic heart failure (CHF) and other forms of chronic cardiac dysfunction (CCD) may be related to an autonomic imbalance of the sympathetic and parasympathetic nervous systems that, if left untreated, can lead to cardiac arrhythmogenesis, progressively worsening cardiac function and eventual patient death. CHF is pathologically characterized by an elevated neuroexitatory state and is accompanied by physiological indications of impaired arterial and cardiopulmonary baroreflex function with reduced vagal activity.

CHF triggers compensatory activations of the sympathoadrenal (sympathetic) nervous system and the renin-angiotensin-aldosterone hormonal system, which initially helps to compensate for deteriorating heart-pumping function, yet, over time, can promote progressive left ventricular dysfunction and deleterious cardiac remodeling. Patients suffering from CHF are at increased risk of tachyarrhythmias, such as atrial fibrillation (AF), ventricular tachyarrhythmias (ventricular tachycardia (VT) and ventricular fibrillation (VF)), and atrial flutter, particularly when the underlying morbidity is a form of coronary artery disease, cardiomyopathy, mitral valve prolapse, or other valvular heart disease. Sympathoadrenal activation also significantly increases the risk and severity of tachyarrhythmias due to neuronal action of the sympathetic nerve fibers in, on, or around the heart and through the release of epinephrine (adrenaline), which can exacerbate an already-elevated heart rate.

The standard of care for managing CCD in general continues to evolve. For instance, new therapeutic approaches that employ electrical stimulation of neural structures that directly address the underlying cardiac autonomic nervous system imbalance and dysregulation have been proposed. In one form, controlled stimulation of the cervical vagus nerve beneficially modulates cardiovascular regulatory function. Vagus nerve stimulation (VNS) has been used for the clinical treatment of drug-refractory epilepsy and depression, and more recently has been proposed as a therapeutic treatment of heart conditions such as CHF. For instance, VNS has been demonstrated in canine studies as efficacious in simulated treatment of AF and heart failure, such as described in Zhang et al., “Chronic Vagus Nerve Stimulation Improves Autonomic Control and Attenuates Systemic Inflammation and Heart Failure Progression in a Canine High-Rate Pacing Model,” Circ Heart Fail 2009, 2, pp. 692-699 (Sep. 22, 2009), the disclosure of which is incorporated by reference. The results of a multi-center open-label phase II study in which chronic VNS was utilized for CHF patients with severe systolic dysfunction is described in De Ferrari et al., “Chronic Vagus Nerve Stimulation: A New and Promising Therapeutic Approach for Chronic Heart Failure,” European Heart Journal, 32, pp. 847-855 (Oct. 28, 2010).

VNS therapy commonly requires implantation of a neurostimulator, a surgical procedure requiring several weeks of recovery before the neurostimulator can be activated and a patient can start receiving VNS therapy. Even after the recovery and activation of the neurostimulator, a full therapeutic dose of VNS is not immediately delivered to the patient to avoid causing significant patient discomfort and other undesirable side effects. Instead, to allow the patient to adjust to the VNS therapy, a titration process is utilized in which the intensity is gradually increased over a period of time under a control of a physician, with the patient given time between successive increases in VNS therapy intensity to adapt to the new intensity. As stimulation is chronically applied at each new intensity level, the patient's tolerance threshold, or tolerance zone boundary, gradually increases, allowing for an increase in intensity during subsequent titration sessions. The titration process can take significantly longer in practice because the increase in intensity is generally performed by a physician or other healthcare provider, and thus, for every step in the titration process to take place, the patient has to visit the provider's office to have the titration performed. Scheduling conflicts in the provider's office may increase the time between titration sessions, thereby extending the overall titration process, during which the patient in need of VNS does not receive the VNS at the full therapeutic intensity.

For patients receiving VNS therapy for the treatment of epilepsy, a titration process that continues over an extended period of time, such as six to twelve months, may be somewhat acceptable because the patient's health condition typically would not worsen in that period of time. However, for patients being treated for other health conditions, such as CHF, the patient's condition may degrade rapidly if left untreated. As a result, there is a much greater urgency to completing the VNS titration process when treating a patient with a time-sensitive condition, such as CHF.

Accordingly, there is a need remains for an approach to efficiently providing neurostimulation therapy, and, in particular, to neurostimulation therapy for treating chronic cardiac dysfunction and other conditions.

SUMMARY

Systems and methods are provided for delivering neurostimulation therapies to patients for treating chronic heart failure. A titration process is used to gradually increase the stimulation intensity to a desired therapeutic level. This titration process can minimize the amount of time required to complete titration so as to begin delivery of the stimulation at therapeutically desirable levels.

In accordance with embodiments of the present invention, a method of operating an implantable medical device (IMD) comprising a neurostimulator coupled to an electrode assembly is provided. The neurostimulator has a stimulation parameter set comprising an output current, a frequency, a pulse width, and a duty cycle. The method comprises: at an initial titration session, activating the IMD to generate a stimulation signal having an initial stimulation parameter set, said initial parameter set comprising an initial output current, an initial frequency, an initial pulse width, and an initial duty cycle; and performing a titration process. The titration process comprises: increasing the output current of the stimulation signal until the stimulation signal comprises a target output current, the patient exceeds a side effect tolerance zone boundary, or adequate adaptation is achieved; and after the stimulation signal comprises the target output current, increasing one or more of the frequency, pulse width, and duty cycle.

In accordance with embodiments of the present invention, a method of operating an implantable medical device (IMD) comprising a neurostimulator coupled to an electrode assembly is provided. The neurostimulator has a stimulation parameter set comprising an output current, a frequency, a pulse width, and a duty cycle. The method comprises: at an initial titration session, activating the IMD to generate a stimulation signal having an initial stimulation parameter set, said initial parameter set comprising an initial output current, an initial frequency, an initial pulse width, and an initial duty cycle; and performing a titration process. The titration process comprises: while maintaining the frequency, pulse width, and duty cycle of the stimulation signal, increasing the output current of the stimulation signal; wherein if the stimulation signal reaches a target output current, then increasing the frequency, pulse width, and duty cycle of the stimulation signal.

In accordance with embodiments of the present invention, a neurostimulation system is provided, comprising: an electrode assembly; a neurostimulator coupled to the electrode assembly, said neurostimulator adapted to deliver a stimulation signal to a patient, said stimulation signal comprising an ON time and an OFF time; a physiological sensor configured to acquire a physiological signal from the patient; and a control system coupled to the neurostimulator and the physiological sensor. The control system is programmed to: determine a physiological response to the stimulation signal by monitoring a baseline signal acquired by the physiological sensor during the OFF time periods of the stimulation signal and monitoring a response signal acquired by the physiological sensor during the ON time periods of the stimulation signal; and perform a titration process. The titration process comprises: increasing an output current of the stimulation signal until the stimulation signal comprises a target output current, the patient exceeds a side effect tolerance zone boundary, or adequate adaptation is achieved; and after the stimulation signal comprises the target output current, increasing a frequency, pulse width, and duty cycle of the stimulation signal until the patient exceeds a side effect tolerance zone boundary or adequate adaptation is achieved.

Still other embodiments of the present invention will become readily apparent to those skilled in the art from the following detailed description, wherein are described embodiments by way of illustrating the best mode contemplated for carrying out the invention. As will be realized, the invention is capable of other and different embodiments and its several details are capable of modifications in various obvious respects, all without departing from the spirit and the scope of the present invention. Accordingly, the drawings and detailed description are to be regarded as illustrative in nature and not as restrictive.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a front anatomical diagram showing, by way of example, placement of an implantable vagus stimulation device in a male patient, in accordance with one embodiment.

FIGS. 2A and 2B are diagrams respectively showing the implantable neurostimulator and the simulation therapy lead of FIG. 1.

FIG. 3 is a diagram showing an external programmer for use with the implantable neurostimulator of FIG. 1.

FIG. 4 is a diagram showing electrodes provided as on the stimulation therapy lead of FIG. 2 in place on a vagus nerve in situ.

FIG. 5 is a graph showing, by way of example, the relationship between the targeted therapeutic efficacy and the extent of potential side effects resulting from use of the implantable neurostimulator of FIG. 1.

FIG. 6 is a graph showing, by way of example, the optimal duty cycle range based on the intersection depicted in FIG. 3.

FIG. 7 is a timing diagram showing, by way of example, a stimulation cycle and an inhibition cycle of VNS as provided by implantable neurostimulator of FIG. 1.

FIGS. 8A-8C are illustrative charts reflecting a heart rate response to gradually increased stimulation intensity at different frequencies.

FIG. 9 illustrates a method for delivering vagus nerve stimulation therapy.

FIG. 10 illustrates a titration process in accordance with embodiments of the present invention.

FIGS. 11A-11B are block diagrams of neurostimulation systems in accordance with embodiments of the present invention.

 DETAILED DESCRIPTION

CHF and other cardiovascular diseases cause derangement of autonomic control of the cardiovascular system, favoring increased sympathetic and decreased parasympathetic central outflow. These changes are accompanied by elevation of basal heart rate arising from chronic sympathetic hyperactivation along the neurocardiac axis.

The vagus nerve is a diverse nerve trunk that contains both sympathetic and parasympathetic fibers, and both afferent and efferent fibers. These fibers have different diameters and myelination, and subsequently have different activation thresholds. This results in a graded response as intensity is increased. Low intensity stimulation results in a progressively greater tachycardia, which then diminishes and is replaced with a progressively greater bradycardia response as intensity is further increased. Peripheral neurostimulation therapies that target the fluctuations of the autonomic nervous system have been shown to improve clinical outcomes in some patients. Specifically, autonomic regulation therapy results in simultaneous creation and propagation of efferent and afferent action potentials within nerve fibers comprising the cervical vagus nerve. The therapy directly improves autonomic balance by engaging both medullary and cardiovascular reflex control components of the autonomic nervous system. Upon stimulation of the cervical vagus nerve, action potentials propagate away from the stimulation site in two directions, efferently toward the heart and afferently toward the brain. Efferent action potentials influence the intrinsic cardiac nervous system and the heart and other organ systems, while afferent action potentials influence central elements of the nervous system.

An implantable vagus nerve stimulator, such as used to treat drug-refractory epilepsy and depression, can be adapted for use in managing chronic cardiac dysfunction (CCD) through therapeutic bi-directional vagus nerve stimulation. FIG. 1 is a front anatomical diagram showing, by way of example, placement of an implantable medical device (e.g., a vagus nerve stimulation (VNS) system 11, as shown in FIG. 1) in a male patient 10, in accordance with embodiments of the present invention. The VNS provided through the stimulation system 11 operates under several mechanisms of action. These mechanisms include increasing parasympathetic outflow and inhibiting sympathetic effects by inhibiting norepinephrine release and adrenergic receptor activation. More importantly, VNS triggers the release of the endogenous neurotransmitter acetylcholine and other peptidergic substances into the synaptic cleft, which has several beneficial anti-arrhythmic, anti-apoptotic, and anti-inflammatory effects as well as beneficial effects at the level of the central nervous system.

The implantable vagus stimulation system 11 comprises an implantable neurostimulator or pulse generator 12 and a stimulating nerve electrode assembly 125. The stimulating nerve electrode assembly 125, preferably comprising at least an electrode pair, is conductively connected to the distal end of an insulated, electrically conductive lead assembly 13 and electrodes 14. The electrodes 14 may be provided in a variety of forms, such as, e.g., helical electrodes, probe electrodes, cuff electrodes, as well as other types of electrodes.

The implantable vagus stimulation system 11 can be remotely accessed following implant through an external programmer, such as the programmer 40 shown in FIG. 3 and described in further detail below. The programmer 40 can be used by healthcare professionals to check and program the neurostimulator 12 after implantation in the patient 10 and to adjust stimulation parameters during the initial stimulation titration process. In some embodiments, an external magnet may provide basic controls, such as described in commonly assigned U.S. Pat. No. 8,600,505, entitled “Implantable Device For Facilitating Control Of Electrical Stimulation Of Cervical Vagus Nerves For Treatment Of Chronic Cardiac Dysfunction,” the disclosure of which is incorporated by reference. For further example, an electromagnetic controller may enable the patient 10 or healthcare professional to interact with the implanted neurostimulator 12 to exercise increased control over therapy delivery and suspension, such as described in commonly-assigned U.S. Pat. No. 8,571,654, entitled “Vagus Nerve Neurostimulator With Multiple Patient-Selectable Modes For Treating Chronic Cardiac Dysfunction,” the disclosure of which is incorporated by reference. For further example, an external programmer may communicate with the neurostimulation system 11 via other wired or wireless communication methods, such as, e.g., wireless RF transmission. Together, the implantable vagus stimulation system 11 and one or more of the external components form a VNS therapeutic delivery system.

The neurostimulator 12 is typically implanted in the patient's right or left pectoral region generally on the same side (ipsilateral) as the vagus nerve 15, 16 to be stimulated, although other neurostimulator-vagus nerve configurations, including contra-lateral and bi-lateral are possible. A vagus nerve typically comprises two branches that extend from the brain stem respectively down the left side and right side of the patient, as seen in FIG. 1. The electrodes 14 are generally implanted on the vagus nerve 15, 16 about halfway between the clavicle 19a-b and the mastoid process. The electrodes may be implanted on either the left or right side. The lead assembly 13 and electrodes 14 are implanted by first exposing the carotid sheath and chosen branch of the vagus nerve 15, 16 through a latero-cervical incision (perpendicular to the long axis of the spine) on the ipsilateral side of the patient's neck 18. The helical electrodes 14 are then placed onto the exposed nerve sheath and tethered. A subcutaneous tunnel is formed between the respective implantation sites of the neurostimulator 12 and helical electrodes 14, through which the lead assembly 13 is guided to the neurostimulator 12 and securely connected.

In one embodiment, the neural stimulation is provided as a low level maintenance dose independent of cardiac cycle. The stimulation system 11 bi-directionally stimulates either the left vagus nerve 15 or the right vagus nerve 16. However, it is contemplated that multiple electrodes 14 and multiple leads 13 could be utilized to stimulate simultaneously, alternatively or in other various combinations. Stimulation may be through multimodal application of continuously-cycling, intermittent and periodic electrical stimuli, which are parametrically defined through stored stimulation parameters and timing cycles. Both sympathetic and parasympathetic nerve fibers in the vagosympathetic complex are stimulated. A study of the relationship between cardiac autonomic nerve activity and blood pressure changes in ambulatory dogs is described in J. Hellyer et al., “Autonomic Nerve Activity and Blood Pressure in Ambulatory Dogs,” Heart Rhythm, Vol. 11(2), pp. 307-313 (February 2014). Generally, cervical vagus nerve stimulation results in propagation of action potentials from the site of stimulation in a bi-directional manner. The application of bi-directional propagation in both afferent and efferent directions of action potentials within neuronal fibers comprising the cervical vagus nerve improves cardiac autonomic balance. Afferent action potentials propagate toward the parasympathetic nervous system's origin in the medulla in the nucleus ambiguus, nucleus tractus solitarius, and the dorsal motor nucleus, as well as towards the sympathetic nervous system's origin in the intermediolateral cell column of the spinal cord. Efferent action potentials propagate toward the heart 17 to activate the components of the heart's intrinsic nervous system. Either the left or right vagus nerve 15, 16 can be stimulated by the stimulation system 11. The right vagus nerve 16 has a moderately lower (approximately 30%) stimulation threshold than the left vagus nerve 15 for heart rate effects at the same stimulation frequency and pulse width.

The VNS therapy is delivered autonomously to the patient's vagus nerve 15, 16 through three implanted components that include a neurostimulator 12, lead assembly 13, and electrodes 14. FIGS. 2A and 2B are diagrams respectively showing the implantable neurostimulator 12 and the stimulation lead assembly 13 of FIG. 1. In one embodiment, the neurostimulator 12 can be adapted from a VNS Therapy Demipulse Model 103 or AspireSR Model 106 pulse generator, manufactured and sold by Cyberonics, Inc., Houston, Tex., although other manufactures and types of implantable VNS neurostimulators could also be used. The stimulation lead assembly 13 and electrodes 14 are generally fabricated as a combined assembly and can be adapted from a Model 302 lead, PerenniaDURA Model 303 lead, or PerenniaFLEX Model 304 lead, also manufactured and sold by Cyberonics, Inc., in two sizes based, for example, on a helical electrode inner diameter, although other manufactures and types of single-pin receptacle-compatible therapy leads and electrodes could also be used.

Referring first to FIG. 2A, the system 20 may be configured to provide multimodal vagus nerve stimulation. In a maintenance mode, the neurostimulator 12 is parametrically programmed to deliver continuously-cycling, intermittent and periodic ON-OFF cycles of VNS. Such delivery produces action potentials in the underlying nerves that propagate bi-directionally, both afferently and efferently.

The neurostimulator 12 includes an electrical pulse generator that is tuned to improve autonomic regulatory function by triggering action potentials that propagate both afferently and efferently within the vagus nerve 15, 16. The neurostimulator 12 is enclosed in a hermetically sealed housing 21 constructed of a biocompatible material, such as titanium. The housing 21 contains electronic circuitry 22 powered by a battery 23, such as a lithium carbon monofluoride primary battery or a rechargeable secondary cell battery. The electronic circuitry 22 may be implemented using complementary metal oxide semiconductor integrated circuits that include a microprocessor controller that executes a control program according to stored stimulation parameters and timing cycles; a voltage regulator that regulates system power; logic and control circuitry, including a recordable memory 29 within which the stimulation parameters are stored, that controls overall pulse generator function, receives and implements programming commands from the external programmer, or other external source, collects and stores telemetry information, processes sensory input, and controls scheduled and sensory-based therapy outputs; a transceiver that remotely communicates with the external programmer using radio frequency signals; an antenna, which receives programming instructions and transmits the telemetry information to the external programmer; and a reed switch 30 that provides remote access to the operation of the neurostimulator 12 using an external programmer, a simple patient magnet, or an electromagnetic controller. The recordable memory 29 can include both volatile (dynamic) and non-volatile/persistent (static) forms of memory, such as firmware within which the stimulation parameters and timing cycles can be stored. Other electronic circuitry and components are possible.

The neurostimulator 12 includes a header 24 to securely receive and connect to the lead assembly 13. In one embodiment, the header 24 encloses a receptacle 25 into which a single pin for the lead assembly 13 can be received, although two or more receptacles could also be provided, along with the corresponding electronic circuitry 22. The header 24 internally includes a lead connector block (not shown) and a set of screws 26.

In some embodiments, the housing 21 may also contain a heart rate sensor 31 that is electrically interfaced with the logic and control circuitry, which receives the patient's sensed heart rate as sensory inputs. The heart rate sensor 31 monitors heart rate using an ECG-type electrode. Through the electrode, the patient's heart beat can be sensed by detecting ventricular depolarization. In a further embodiment, a plurality of electrodes can be used to sense voltage differentials between electrode pairs, which can undergo signal processing for cardiac physiological measures, for instance, detection of the P-wave, QRS complex, and T-wave. The heart rate sensor 31 provides the sensed heart rate to the control and logic circuitry as sensory inputs that can be used to determine the onset or presence of arrhythmias, particularly VT, and/or to monitor and record changes in the patient's heart rate over time or in response to applied stimulation signals.

Referring next to FIG. 2B, the lead assembly 13 delivers an electrical signal from the neurostimulator 12 to the vagus nerve 15, 16 via the electrodes 14. On a proximal end, the lead assembly 13 has a lead connector 27 that transitions an insulated electrical lead body to a metal connector pin 28. During implantation, the connector pin 28 is guided through the receptacle 25 into the header 24 and securely fastened in place using the set screws 26 to electrically couple the lead assembly 13 to the neurostimulator 12. On a distal end, the lead assembly 13 terminates with the electrode 14, which bifurcates into a pair of anodic and cathodic electrodes 62 (as further described infra with reference to FIG. 4). In one embodiment, the lead connector 27 is manufactured using silicone and the connector pin 28 is made of stainless steel, although other suitable materials could be used, as well. The insulated lead body 13 utilizes a silicone-insulated alloy conductor material.

In some embodiments, the electrodes 14 are helical and placed around the cervical vagus nerve 15, 16 at the location below where the superior and inferior cardiac branches separate from the cervical vagus nerve. In alternative embodiments, the helical electrodes may be placed at a location above where one or both of the superior and inferior cardiac branches separate from the cervical vagus nerve. In one embodiment, the helical electrodes 14 are positioned around the patient's vagus nerve oriented with the end of the helical electrodes 14 facing the patient's head. In an alternate embodiment, the helical electrodes 14 are positioned around the patient's vagus nerve 15, 16 oriented with the end of the helical electrodes 14 facing the patient's heart 17. At the distal end, the insulated electrical lead body 13 is bifurcated into a pair of lead bodies that are connected to a pair of electrodes. The polarity of the electrodes could be configured into a monopolar cathode, a proximal anode and a distal cathode, or a proximal cathode and a distal anode.

The neurostimulator 12 may be interrogated prior to implantation and throughout the therapeutic period with a healthcare provider-operable control system comprising an external programmer and programming wand (shown in FIG. 3) for checking proper operation, downloading recorded data, diagnosing problems, and programming operational parameters, such as described in commonly-assigned U.S. Pat. Nos. 8,600,505 and 8,571,654, cited supra. FIG. 3 is a diagram showing an external programmer 40 for use with the implantable neurostimulator 12 of FIG. 1. The external programmer 40 includes a healthcare provider operable programming computer 41 and a programming wand 42. Generally, use of the external programmer is restricted to healthcare providers, while more limited manual control is provided to the patient through “magnet mode.”

In one embodiment, the external programmer 40 executes application software 45 specifically designed to interrogate the neurostimulator 12. The programming computer 41 interfaces to the programming wand 42 through a wired or wireless data connection. The programming wand 42 can be adapted from a Model 201 Programming Wand, manufactured and sold by Cyberonics, Inc., and the application software 45 can be adapted from the Model 250 Programming Software suite, licensed by Cyberonics, Inc. Other configurations and combinations of external programmer 40, programming wand 42 and application software 45 are possible.

The programming computer 41 can be implemented using a general purpose programmable computer and can be a personal computer, laptop computer, ultrabook computer, netbook computer, handheld computer, tablet computer, smart phone, or other form of computational device. In one embodiment, the programming computer is a tablet computer that may operate under the iOS operating system from Apple Inc., such as the iPad from Apple Inc., or may operate under the Android operating system from Google Inc., such as the Galaxy Tab from Samsung Electronics Co., Ltd. In an alternative embodiment, the programming computer is a personal digital assistant handheld computer operating under the Pocket-PC, Windows Mobile, Windows Phone, Windows RT, or Windows operating systems, licensed by Microsoft Corporation, Redmond, Wash., such as the Surface from Microsoft Corporation, the Dell Axim XS and X50 personal data assistants, sold by Dell, Inc., Round Top, Tex., the HP Jornada personal data assistant, sold by Hewlett-Packard Company, Palo Alto, Tex. The programming computer 41 functions through those components conventionally found in such devices, including, for instance, a central processing unit, volatile and persistent memory, touch-sensitive display, control buttons, peripheral input and output ports, and network interface. The computer 41 operates under the control of the application software 45, which is executed as program code as a series of process or method modules or steps by the programmed computer hardware. Other assemblages or configurations of computer hardware, firmware, and software are possible.

Operationally, the programming computer 41, when connected to a neurostimulator 12 through wireless telemetry using the programming wand 42, can be used by a healthcare provider to remotely interrogate the neurostimulator 12 and modify stored stimulation parameters. The programming wand 42 provides data conversion between the digital data accepted by and output from the programming computer and the radio frequency signal format that is required for communication with the neurostimulator 12. The programming computer 41 may further be configured to receive inputs, such as physiological signals received from patient sensors (e.g., implanted or external). These sensors may be configured to monitor one or more physiological signals, e.g., vital signs, such as body temperature, pulse rate, respiration rate, blood pressure, etc. These sensors may be coupled directly to the programming computer 41 or may be coupled to another instrument or computing device which receives the sensor input and transmits the input to the programming computer 41. The programming computer 41 may monitor, record, and/or respond to the physiological signals in order to effectuate stimulation delivery in accordance with embodiments of the present invention.

The healthcare provider operates the programming computer 41 through a user interface that includes a set of input controls 43 and a visual display 44, which could be touch-sensitive, upon which to monitor progress, view downloaded telemetry and recorded physiology, and review and modify programmable stimulation parameters. The telemetry can include reports on device history that provide patient identifier, implant date, model number, serial number, magnet activations, total ON time, total operating time, manufacturing date, and device settings and stimulation statistics and on device diagnostics that include patient identifier, model identifier, serial number, firmware build number, implant date, communication status, output current status, measured current delivered, lead impedance, and battery status. Other kinds of telemetry or telemetry reports are possible.

During interrogation, the programming wand 42 is held by its handle 46 and the bottom surface 47 of the programming wand 42 is placed on the patient's chest over the location of the implanted neurostimulator 12. A set of indicator lights 49 can assist with proper positioning of the wand and a set of input controls 48 enable the programming wand 42 to be operated directly, rather than requiring the healthcare provider to awkwardly coordinate physical wand manipulation with control inputs via the programming computer 41. The sending of programming instructions and receipt of telemetry information occur wirelessly through radio frequency signal interfacing. Other programming computer and programming wand operations are possible.

FIG. 4 is a diagram showing the helical electrodes 14 provided as on the stimulation lead assembly 13 of FIG. 2 in place on a vagus nerve 15, 16 in situ 50. Although described with reference to a specific manner and orientation of implantation, the specific surgical approach and implantation site selection particulars may vary, depending upon physician discretion and patient physical structure.

Under one embodiment, helical electrodes 14 may be positioned on the patient's vagus nerve 61 oriented with the end of the helical electrodes 14 facing the patient's head. At the distal end, the insulated electrical lead body 13 is bifurcated into a pair of lead bodies 57, 58 that are connected to a pair of electrodes 51, 52. The polarity of the electrodes 51, 52 could be configured into a monopolar cathode, a proximal anode and a distal cathode, or a proximal cathode and a distal anode. In addition, an anchor tether 53 is fastened over the lead bodies 57, 58 that maintains the helical electrodes' position on the vagus nerve 61 following implant. In one embodiment, the conductors of the electrodes 51, 52 are manufactured using a platinum and iridium alloy, while the helical materials of the electrodes 51, 52 and the anchor tether 53 are a silicone elastomer.

During surgery, the electrodes 51, 52 and the anchor tether 53 are coiled around the vagus nerve 61 proximal to the patient's head, each with the assistance of a pair of sutures 54, 55, 56, made of polyester or other suitable material, which help the surgeon to spread apart the respective helices. The lead bodies 57, 58 of the electrodes 51, 52 are oriented distal to the patient's head and aligned parallel to each other and to the vagus nerve 61. A strain relief bend 60 can be formed on the distal end with the insulated electrical lead body 13 aligned, for example, parallel to the helical electrodes 14 and attached to the adjacent fascia by a plurality of tie-downs 59a-b.

The neurostimulator 12 delivers VNS under control of the electronic circuitry 22. The stored stimulation parameters are programmable. Each stimulation parameter can be independently programmed to define the characteristics of the cycles of therapeutic stimulation and inhibition to ensure optimal stimulation for a patient 10. The programmable stimulation parameters include output current, signal frequency, pulse width, signal ON time, signal OFF time, magnet activation (for VNS specifically triggered by “magnet mode”), and reset parameters. Other programmable parameters are possible. In addition, sets or “profiles” of preselected stimulation parameters can be provided to physicians with the external programmer and fine-tuned to a patient's physiological requirements prior to being programmed into the neurostimulator 12, such as described in commonly-assigned U.S. patent application entitled “Computer-Implemented System and Method for Selecting Therapy Profiles of Electrical Stimulation of Cervical Vagus Nerves for Treatment of Chronic Cardiac Dysfunction,” Ser. No. 13/314,138, filed on Dec. 7, 2011, published as U.S. Patent Publication no. 2013-0158618 A1, pending, the disclosure of which is incorporated by reference.

Therapeutically, the VNS may be delivered as a multimodal set of therapeutic doses, which are system output behaviors that are pre-specified within the neurostimulator 12 through the stored stimulation parameters and timing cycles implemented in firmware and executed by the microprocessor controller. The therapeutic doses include a maintenance dose that includes continuously-cycling, intermittent and periodic cycles of electrical stimulation during periods in which the pulse amplitude is greater than 0 mA (“therapy ON”) and during periods in which the pulse amplitude is 0 mA (“therapy OFF”).

The neurostimulator 12 can operate either with or without an integrated heart rate sensor, such as respectively described in commonly-assigned U.S. Pat. No. 8,577,458, entitled “Implantable Device for Providing Electrical Stimulation of Cervical Vagus Nerves for Treatment of Chronic Cardiac Dysfunction with Leadless Heart Rate Monitoring,” and U.S. patent application, entitled “Implantable Device for Providing Electrical Stimulation of Cervical Vagus Nerves for Treatment of Chronic Cardiac Dysfunction,” Ser. No. 13/314,119, filed on Dec. 7, 2011, pending, the disclosures of which are hereby incorporated by reference herein in their entirety. Additionally, where an integrated leadless heart rate monitor is available, the neurostimulator 12 can provide autonomic cardiovascular drive evaluation and self-controlled titration, such as respectively described in commonly-assigned U.S. patent application entitled “Implantable Device for Evaluating Autonomic Cardiovascular Drive in a Patient Suffering from Chronic Cardiac Dysfunction,” Ser. No. 13/314,133, filed on Dec. 7, 2011, U.S. Patent Publication No. 2013-0158616 A1, pending, and U.S. patent application entitled “Implantable Device for Providing Electrical Stimulation of Cervical Vagus Nerves for Treatment of Chronic Cardiac Dysfunction with Bounded Titration,” Ser. No. 13/314,135, filed on Dec. 7, 2011, U.S. Patent Publication No. 2013-0158617 A1, pending, the disclosures of which are incorporated by reference. Finally, the neurostimulator 12 can be used to counter natural circadian sympathetic surge upon awakening and manage the risk of cardiac arrhythmias during or attendant to sleep, particularly sleep apneic episodes, such as respectively described in commonly-assigned U.S. patent application entitled “Implantable Neurostimulator-Implemented Method For Enhancing Heart Failure Patient Awakening Through Vagus Nerve Stimulation,” Ser. No. 13/673,811, filed on Nov. 9, 2012, pending, the disclosure of which is incorporated by reference.

The VNS stimulation signal may be delivered as a therapy in a maintenance dose having an intensity that is insufficient to elicit undesirable side effects, such as cardiac arrhythmias. The VNS can be delivered with a periodic duty cycle in the range of 2% to 89% with a preferred range of around 4% to 36% that is delivered as a low intensity maintenance dose. Alternatively, the low intensity maintenance dose may comprise a narrow range approximately at 17.5%, such as around 15% to 25%. The selection of duty cycle is a tradeoff among competing medical considerations. The duty cycle is determined by dividing the stimulation ON time by the sum of the ON and OFF times of the neurostimulator 12 during a single ON-OFF cycle. However, the stimulation time may also need to include ramp-up time and ramp-down time, where the stimulation frequency exceeds a minimum threshold (as further described infra with reference to FIG. 7).

FIG. 5 is a graph 70 showing, by way of example, the relationship between the targeted therapeutic efficacy 73 and the extent of potential side effects 74 resulting from use of the implantable neurostimulator 12 of FIG. 1, after the patient has completed the titration process. The graph in FIG. 5 provides an illustration of the failure of increased stimulation intensity to provide additional therapeutic benefit, once the stimulation parameters have reached the neural fulcrum zone, as will be described in greater detail below with respect to FIG. 8. As shown in FIG. 5, the x-axis represents the duty cycle 71. The duty cycle is determined by dividing the stimulation ON time by the sum of the ON and OFF times of the neurostimulator 12 during a single ON-OFF cycle. However, the stimulation time may also include ramp-up time and ramp-down time, where the stimulation frequency exceeds a minimum threshold (as further described infra with reference to FIG. 7). When including the ramp-up and ramp-down times, the total duty cycle may be calculated as the ON time plus the ramp-up and ramp-down times divided by the OFF time, ON time, and ramp-up and ramp-down times, and may be, e.g., between 15% and 30%, and more specifically approximately 23%. The y-axis represents physiological response 72 to VNS therapy. The physiological response 72 can be expressed quantitatively for a given duty cycle 71 as a function of the targeted therapeutic efficacy 73 and the extent of potential side effects 74, as described infra. The maximum level of physiological response 72 (“max”) signifies the highest point of targeted therapeutic efficacy 73 or potential side effects 74.

Targeted therapeutic efficacy 73 and the extent of potential side effects 74 can be expressed as functions of duty cycle 71 and physiological response 72. The targeted therapeutic efficacy 73 represents the intended effectiveness of VNS in provoking a beneficial physiological response for a given duty cycle and can be quantified by assigning values to the various acute and chronic factors that contribute to the physiological response 72 of the patient 10 due to the delivery of therapeutic VNS. Acute factors that contribute to the targeted therapeutic efficacy 73 include beneficial changes in heart rate variability and increased coronary flow, reduction in cardiac workload through vasodilation, and improvement in left ventricular relaxation. Chronic factors that contribute to the targeted therapeutic efficacy 73 include improved cardiovascular regulatory function, as well as decreased negative cytokine production, increased baroreflex sensitivity, increased respiratory gas exchange efficiency, favorable gene expression, renin-angiotensin-aldosterone system down-regulation, anti-arrhythmic, anti-apoptotic, and ectopy-reducing anti-inflammatory effects. These contributing factors can be combined in any manner to express the relative level of targeted therapeutic efficacy 73, including weighting particular effects more heavily than others or applying statistical or numeric functions based directly on or derived from observed physiological changes. Empirically, targeted therapeutic efficacy 73 steeply increases beginning at around a 5% duty cycle, and levels off in a plateau near the maximum level of physiological response at around a 30% duty cycle. Thereafter, targeted therapeutic efficacy 73 begins decreasing at around a 50% duty cycle and continues in a plateau near a 25% physiological response through the maximum 100% duty cycle.

The intersection 75 of the targeted therapeutic efficacy 73 and the extent of potential side effects 74 represents one optimal duty cycle range for VNS. FIG. 6 is a graph 80 showing, by way of example, the optimal duty cycle range 83 based on the intersection 75 depicted in FIG. 5. The x-axis represents the duty cycle 81 as a percentage of stimulation time over stimulation time plus inhibition time. The y-axis represents therapeutic points 82 reached in operating the neurostimulator 12 at a given duty cycle 81. The optimal duty range 83 is a function 84 of the intersection 75 of the targeted therapeutic efficacy 73 and the extent of potential side effects 74. The therapeutic operating points 82 can be expressed quantitatively for a given duty cycle 81 as a function of the values of the targeted therapeutic efficacy 73 and the extent of potential side effects 74 at their point of intersection in the graph 70 of FIG. 5. The optimal therapeutic operating point 85 (“max”) signifies a tradeoff that occurs at the point of highest targeted therapeutic efficacy 73 in light of lowest potential side effects 74 and that point will typically be found within the range of a 5% to 30% duty cycle 81. Other expressions of duty cycles and related factors are possible.

Therapeutically and in the absence of patient physiology of possible medical concern, such as cardiac arrhythmias, VNS is delivered in a low level maintenance dose that uses alternating cycles of stimuli application (ON) and stimuli inhibition (OFF) that are tuned to activate both afferent and efferent pathways. Stimulation results in parasympathetic activation and sympathetic inhibition, both through centrally-mediated pathways and through efferent activation of preganglionic neurons and local circuit neurons. FIG. 7 is a timing diagram showing, by way of example, a stimulation cycle and an inhibition cycle of VNS 90, as provided by implantable neurostimulator 12 of FIG. 1. The stimulation parameters enable the electrical stimulation pulse output by the neurostimulator 12 to be varied by both amplitude (output current 96) and duration (pulse width 94). The number of output pulses delivered per second determines the signal frequency 93. In one embodiment, a pulse width in the range of 100 to 250 μsec delivers between 0.02 mA and 50 mA of output current at a signal frequency of about 10 Hz, although other therapeutic values could be used as appropriate. In general, the stimulation signal delivered to the patient may be defined by a stimulation parameter set comprising at least an amplitude, a frequency, a pulse width, and a duty cycle.

In one embodiment, the stimulation time is considered the time period during which the neurostimulator 12 is ON and delivering pulses of stimulation, and the OFF time is considered the time period occurring in-between stimulation times during which the neurostimulator 12 is OFF and inhibited from delivering stimulation.

In another embodiment, as shown in FIG. 7, the neurostimulator 12 implements a stimulation time 91 comprising an ON time 92, a ramp-up time 97 and a ramp-down time 98 that respectively precede and follow the ON time 92. Under this embodiment, the ON time 92 is considered to be a time during which the neurostimulator 12 is ON and delivering pulses of stimulation at the full output current 96. Under this embodiment, the OFF time 95 is considered to comprise the ramp-up time 97 and ramp-down time 98, which are used when the stimulation frequency is at least 10 Hz, although other minimum thresholds could be used, and both ramp-up and ramp-down times 97, 98 last two seconds, although other time periods could also be used. The ramp-up time 97 and ramp-down time 98 allow the strength of the output current 96 of each output pulse to be gradually increased and decreased, thereby avoiding deleterious reflex behavior due to sudden delivery or inhibition of stimulation at a programmed intensity.

Therapeutic vagus neural stimulation has been shown to provide cardioprotective effects. Although delivered in a maintenance dose having an intensity that is insufficient to elicit undesirable side effects, such as cardiac arrhythmias, ataxia, coughing, hoarseness, throat irritation, voice alteration, or dyspnea, therapeutic VNS can nevertheless potentially ameliorate pathological tachyarrhythmias in some patients. Although VNS has been shown to decrease defibrillation threshold, VNS has not been shown to terminate VF in the absence of defibrillation. VNS prolongs ventricular action potential duration, so may be effective in terminating VT. In addition, the effect of VNS on the AV node may be beneficial in patients with AF by slowing conduction to the ventricles and controlling ventricular rate.

Neural Fulcrum Zone

As described above, autonomic regulation therapy results in simultaneous creation of action potentials that simultaneously propagate away from the stimulation site in afferent and efferent directions within axons comprising the cervical vagus nerve complex. Upon stimulation of the cervical vagus nerve, action potentials propagate away from the stimulation site in two directions, efferently toward the heart and afferently toward the brain. Different parameter settings for the neurostimulator 12 may be adjusted to deliver varying stimulation intensities to the patient. The various stimulation parameter settings for current VNS devices include output current amplitude, signal frequency, pulse width, signal ON time, and signal OFF time.

When delivering neurostimulation therapies to patients, it is generally desirable to avoid stimulation intensities that result in either excessive tachycardia or excessive bradycardia. However, researchers have typically utilized the patient's heart rate changes as a functional response indicator or surrogate for effective recruitment of nerve fibers and engagement of the autonomic nervous system elements responsible for regulation of heart rate, which may be indicative of therapeutic levels of VNS. Some researchers have proposed that heart rate reduction caused by VNS stimulation is itself beneficial to the patient.

In accordance with some embodiments, a neural fulcrum zone is identified, and neurostimulation therapy is delivered within the neural fulcrum zone. This neural fulcrum zone corresponds to a combination of stimulation parameters at which autonomic engagement is achieved but for which a functional response determined by heart rate change is nullified due to the competing effects of afferently and efferently-transmitted action potentials. In this way, the tachycardia-inducing stimulation effects are offset by the bradycardia-inducing effects, thereby minimizing side effects such as significant heart rate changes while providing a therapeutic level of stimulation. One method of identifying the neural fulcrum zone is by delivering a plurality of stimulation signals at a fixed frequency but with one or more other parameter settings changed so as to gradually increase the intensity of the stimulation.

FIGS. 8A-8C provide illustrative charts reflecting the location of the neural fulcrum zone. FIG. 8A is a chart 800 illustrating a heart rate response in response to such a gradually increased intensity at a first frequency, in accordance with embodiments of the present invention. In this chart 800, the x-axis represents the intensity level of the stimulation signal, and the y-axis represents the observed heart rate change from the patient's baseline basal heart rate observed when no stimulation is delivered. In this example, the stimulation intensity is increased by increasing the output current amplitude.

A first set 810 of stimulation signals is delivered at a first frequency (e.g., 10 Hz). Initially, as the intensity (e.g., output current amplitude) is increased, a tachycardia zone 851-1 is observed, during which period, the patient experiences a mild tachycardia. As the intensity continues to be increased for subsequent stimulation signals, the patient's heart rate response begins to decrease and eventually enters a bradycardia zone 853-1, in which a bradycardia response is observed in response to the stimulation signals. As described above, the neural fulcrum zone is a range of stimulation parameters at which the functional effects from afferent activation are balanced with or nullified by the functional effects from efferent activation to avoid extreme heart rate changes while providing therapeutic levels of stimulation. In accordance with some embodiments, the neural fulcrum zone 852-1 can be located by identifying the zone in which the patient's response to stimulation produces either no heart rate change or a mildly decreased heart rate change (e.g., <5% decrease, or a target number of beats per minute). As the intensity of stimulation is further increased at the fixed first frequency, the patient enters an undesirable bradycardia zone 853-1. In these embodiments, the patient's heart rate response is used as an indicator of autonomic engagement. In other embodiments, other physiological responses may be used to indicate the zone of autonomic engagement at which the propagation of efferent and afferent action potentials are balanced, the neural fulcrum zone.

FIG. 8B is a chart 860 illustrating a heart rate response in response to such a gradually increased intensity at two additional frequencies, in accordance with embodiments of the present invention. In this chart 860, the x-axis and y-axis represent the intensity level of the stimulation signal and the observed heart rate change, respectively, as in FIG. 8A, and the first set 810 of stimulation signals from FIG. 8A is also shown.

A second set 820 of stimulation signals is delivered at a second frequency lower than the first frequency (e.g., 5 Hz). Initially, as the intensity (e.g., output current amplitude) is increased, a tachycardia zone 851-2 is observed, during which period, the patient experiences a mild tachycardia. As the intensity continues to be increased for subsequent stimulation signals, the patient's heart rate response begins to decrease and eventually enters a bradycardia zone 853-2, in which a bradycardia response is observed in response to the stimulation signals. The low frequency of the stimulation signal in the second set 820 of stimulation signals limits the functional effects of nerve fiber recruitment and, as a result, the heart response remains relatively limited. Although this low frequency stimulation results in minimal side effects, the stimulation intensity is too low to result in effective recruitment of nerve fibers and engagement of the autonomic nervous system. As a result, a therapeutic level of stimulation is not delivered.

A third set of 830 of stimulation signals is delivered at a third frequency higher than the first and second frequencies (e.g., 20 Hz). As with the first set 810 and second set 820, at lower intensities, the patient first experiences a tachycardia zone 851-3. At this higher frequency, the level of increased heart rate is undesirable. As the intensity is further increased, the heart rate decreases, similar to the decrease at the first and second frequencies but at a much higher rate. The patient first enters the neural fulcrum zone 852-3 and then the undesirable bradycardia zone 853-3. Because the slope of the curve for the third set 830 is much steeper than the second set 820, the region in which the patient's heart rate response is between 0% and −5% (e.g., the neural fulcrum zone 852-3) is much narrower than the neural fulcrum zone 852-2 for the second set 820. Accordingly, when testing different operational parameter settings for a patient by increasing the output current amplitude by incremental steps, it can be more difficult to locate a programmable output current amplitude that falls within the neural fulcrum zone 852-3. When the slope of the heart rate response curve is high, the resulting heart rate may overshoot the neural fulcrum zone and create a situation in which the functional response transitions from the tachycardia zone 851-3 to the undesirable bradycardia zone 853-3 in a single step. At that point, the clinician would need to reduce the amplitude by a smaller increment or reduce the stimulation frequency in order to produce the desired heart rate response for the neural fulcrum zone 852-3.

FIG. 8C is a chart 880 illustrating mean heart rate response surfaces in conscious, normal dogs during 14 second periods of right cervical vagus VNS stimulation ON-time. The heart rate responses shown in z-axis represent the percentage heart rate change from the baseline heart rate at various sets of VNS parameters, with the pulse width the pulse width set at 250 μsec, the pulse amplitude ranging from 0 mA to 3.5 mA (provided by the x-axis) and the pulse frequency ranging from 2 Hz to 20 Hz (provided by the y-axis). Curve 890 roughly represents the range of stimulation amplitude and frequency parameters at which a null response (i.e., 0% heart rate change from baseline) is produced. This null response curve 890 is characterized by the opposition of functional responses (e.g., tachycardia and bradycardia) arising from afferent and efferent activation.

Titration Process

FIG. 9 is a flow diagram showing a method for delivering vagus nerve stimulation therapy, in accordance with embodiments of the present invention. A titration process is used to gradually increase the stimulation intensity to a desired therapeutic level. If the stimulation intensity is increased too quickly before the patient is fully accommodated to the stimulation signal, the patient may experience undesirable side effects, such as coughing, hoarseness, throat irritation, or expiratory reflex. The titration process gradually increases stimulation intensity within a tolerable level, and maintains that intensity for a period of time to permit the patient to adjust to each increase in intensity, thereby gradually increasing the patient's side effect tolerance zone boundary to so as to accommodate subsequent increases in intensity. The titration process continues until adequate adaptation is achieved. As will be described in greater detail below, adequate adaptation is a composite threshold comprising one or more of the following: an acceptable side effect level, a target intensity level, and a target physiological response.

As described above, it may be desirable to minimize the amount of time required to complete the titration process so as to begin delivery of the stimulation at therapeutically desirable levels, particularly when the patient is being treated for an urgent condition such as CHF. In addition, it is desirable to utilize a maintenance dose intensity at the minimum level required to achieve the desired therapeutic effect. This can reduce power requirements for the neurostimulator and reduce patient discomfort.

It has been observed that a patient's side effect profile is more sensitive to the stimulation output current than to the other stimulation parameters, such as frequency, pulse width, and duty cycle. As a result, accommodation to the stimulation output current is a primary factor in completing the titration process. It has also been observed that if the other stimulation parameters are maintained at a level below the target levels, the output current can increased to higher levels without eliciting undesirable side effects that would be result when the other parameters are at the target level. As a result, increasing the target output current while maintaining the other stimulation parameters (pulse width in particular) at reduced levels can result in a faster accommodation and shorter overall titration time than would be achieved by attempting to increase the output current while stimulating at the target pulse width.

In step 901, a stimulation system 11, including a neurostimulator 12, a nerve stimulation lead assembly 13, and a pair of electrodes 14, is implanted in the patient. In step 902, the patient undergoes an optional post-surgery recovery period, during which time the surgical incisions are allowed to heal and no VNS therapy occurs. This period may last, e.g., two weeks post surgery. In step 903, the stimulation therapy process is initiated. During this process, VNS therapy is titrated by adjusting one or more of the stimulation parameters, including output current, pulse width, signal frequency, and duty cycle, as will be described in greater detail below. After the completion of the titration process will determine the stimulation intensity to be used for subsequent maintenance doses delivered in step 904. These maintenance doses may be selected to provide the minimum stimulation intensity necessary to provide the desired therapeutic result.

FIG. 10 is a flow diagram illustrating a titration process 1000 in accordance with embodiments of the present invention. When first initiating the titration process, the neurostimulator 11 is configured to generate a stimulation signal having an initial stimulation parameter set. The initial parameter set may comprise an initial output current, an initial frequency, an initial pulse width, and an initial duty cycle. The various initial parameter settings may vary, but may be selected so that one or more of the parameters are set at levels below a predefined target parameter set level, such that the titration process is used to gradually increase the intensity parameters to achieve adequate adaptation. In some embodiments, the initial frequency is set at the target frequency level, while the initial output current, initial pulse width, and initial duty cycle are set below their respective target levels. In one embodiment, the target parameter set comprises a 10 Hz frequency, 250 μsec pulse width, a duty cycle of 14 sec ON and 1.1 minutes OFF, and an output current of between 1.5 mA-3.0 mA (e.g., 2.5 mA for right side stimulation and 3.0 mA for left side stimulation), and the initial parameter set comprises 10 Hz frequency, 130 μsec pulse width, a duty cycle of 14 sec ON and 1.1 minutes OFF, and an output current of between 0.25 mA-0.5 mA.

In step 1001, the stimulation system delivers stimulation to the patient. If this is the first titration session, then the stimulation would be delivered with the initial stimulation parameter set described above. If this is a subsequent titration session, then the stimulation intensity would remain at the same level at the conclusion of the previous titration session.

In step 1002, the output current is gradually increased until the stimulation results in an intolerable side effect level, the target output current (e.g., 2.5 mA) is reached, or adequate adaptation is achieved. As described above, adequate adaptation is a composite threshold comprising one or more of the following: an acceptable side effect level, a target intensity level, and a target physiological response. In accordance with some embodiments, the target physiological response comprises a target heart rate change during stimulation. The patient's heart rate may be monitored using an implanted or external heart rate monitor, and the patient's heart rate during stimulation is compared to the patient's baseline heart rate to determine the extent of heart rate change. In accordance with some embodiments, the target heart rate change is a heart rate change of between 4% and 5%. If at any point during the titration process 1000 adequate adaptation is achieved, the titration process ends and the stimulation intensity which resulted in the adequate adaptation is used for ongoing maintenance dose therapy delivery.

The output current may be increased in any desired increment, but small increments, e.g., 0.1 mA or 0.25 mA, may be desirable so as to enable more precise adjustments. In some cases, the output current increments may be determined by the neurostimulator's maximum control capability. During the initial titration sessions, it is likely that the patient's side effect tolerance zone boundary will be reached well before the output current reaches the target level or adequate adaptation is achieved. At decision step 1003, if the target output current has not been achieved but the maximum tolerable side effects have been exceeded, the process proceeds to step 1004.

In step 1004, the output current is reduced one increment to bring the side effects within acceptable levels. In addition, the frequency is reduced. In embodiments in which the initial frequency was 10 Hz, in step 1004, the frequency may be reduced, e.g., to 5 Hz or 2 Hz.

Next, in step 1005, the output current is gradually increased again at the reduced frequency level until the stimulation results in an intolerable side effect level or the target output current (e.g., 2.5 mA) is reached. At decision step 1006, if the target output current has not been reached but the maximum tolerable side effects have been exceeded, the process proceeds to step 1007.

In step 1007, the titration session is concluded. The stimulation system may be programmed to continue delivering the stimulation signal at the last parameter settings achieved prior to conclusion of the titration session. After a period of time, another titration session may be initiated and the process returns to step 1001. This can be any period of time sufficient to permit the patient to adjust to the increased stimulation levels. This can be, for example, as little as approximately two or three days, approximately one to two weeks, approximately four to eight weeks, or any other desired period of time.

In some embodiments, the titration sessions are automatically initiated by the stimulation system or initiated by the patient without requiring any intervention by the health care provider. This can eliminate the need for the patient to schedule a subsequent visit to the health care provider, thereby potentially reducing the total amount of time needed for the titration process to complete. In these embodiments, the stimulation system includes a physiological monitor, e.g., an implanted heart rate sensor, that communicates with the stimulation system's control system to enable the control system to detect when the target physiological response has been achieved and conclude the titration process. The stimulation system could further include a patient control input to permit the patient to communicate to the control system that the acceptable side effect level has been exceeded. This control input may comprise an external control magnet that the patient can swipe over the implanted neurostimulator, or other internal or external communication device that the patient can use to provide an input to the control system. In these automatically initiated titration sessions, the stimulation system may be configured to wait a period of time after completing one session before initiating the next session. This period of time may be predetermined, e.g., two or three days.

Returning to decision step 1006, if the target output current has not been reached but the maximum tolerable side effects have been exceeded, the process proceeds to step 1008. In step 1008, the output current is reduced one increment to restore an acceptable side effect condition, and the frequency is gradually increased until the stimulation results in an intolerable side effect level or the target frequency (e.g., 10 Hz) is reached. At decision step 1009, if the target frequency has not been reached but the maximum tolerable side effects have been exceeded, the frequency is reduced to restore an acceptable side effect level and the process proceeds to step 1007. Again, in step 1007, the current titration session is concluded and the stimulation system may be programmed to continue delivering the stimulation signal at the last parameter settings achieved prior to conclusion of the titration session.

At decision step 1009, if the target frequency has been reached before the maximum tolerable side effects have been exceeded, the duty cycle is gradually increased until the stimulation results in an intolerable side effect level or the target duty cycle (e.g., 14 sec ON and 1.1 min OFF) is reached, at which point the process proceeds to step 1007 and the titration session is concluded and ongoing stimulation delivered at the last intensity eliciting acceptable side effect levels.

Returning to decision step 1003, if the target output current has been achieved before the maximum tolerable side effects are exceeded, the process proceeds to step 1011. In step 1011, the pulse width is gradually increased until the stimulation results in an intolerable side effect level or the target pulse width (e.g., 250 μsec) is reached. In some embodiments, before step 1011, the output current is reduced (e.g., by up to 50%), and the pulse width may be increased in step 1011 at that reduced output current. After the target pulse width is achieved, the output current may be restored to the target output current. In other embodiments, the output current may be reduced (or may be retained at the reduced level established prior to step 1011, as described above), and the frequency and duty cycle are gradually increased in step 1013 at that reduced output current. This reduction in output current after achieving the target output current may enable the patient to maintain tolerability with increasing pulse width, frequency, and duty cycle in subsequent titration steps.

At decision step 1012, if the target pulse width has not been achieved before the maximum tolerable side effects have been exceeded, the pulse width is reduced to restore an acceptable side effect level and the process proceeds to step 1007. Again, in step 1007, the current titration session is concluded.

If at decision step 1012, the target pulse width has been achieved before the maximum tolerable side effects have been exceeded, the process proceeds to step 1013. In step 1013, the frequency and duty cycle are increased until the stimulation results in an intolerable side effect level or the target frequency and target duty cycle are reached. The frequency and duty cycle can be increased in step 1012 simultaneously, sequentially, or on an alternating basis.

At decision step 1014, if the target frequency and target duty cycle have not been achieved before the maximum tolerable side effects have been exceeded, the pulse width and/or frequency are reduced to restore an acceptable side effect level and the process continues to step 1007 and the titration session is concluded.

At decision step 1014, if the target pulse width and target frequency have been achieved before the maximum tolerable side effects have been exceeded, all of the stimulation parameters will have reached their target levels and the titration process concludes at step 1015. The stimulation therapy may proceed with the maintenance dose at the target stimulation levels.

In some embodiments, in step 1004, instead of reducing the frequency in order to facilitate increase of the output current, the pulse width may be reduced. For example, embodiments where the target pulse width is 250 μsec, the pulse width may be reduced, e.g., to 150 μsec or less. Then, the method proceeds to step 1005, in which the output current is gradually increased again at the reduced pulse width level until the stimulation results in an intolerable side effect level or the target output current (e.g., 2.5 mA) is reached.

Therapy can also be autonomously titrated by the neurostimulator 12 in which titration progressively occurs in a self-paced, self-monitored fashion. The progression of titration sessions may occur on an autonomous schedule or may be initiated upon receipt of an input from the patient. Ordinarily, the patient 10 is expected to visit his healthcare provider to have the stimulation parameters stored by the neurostimulator 12 in the recordable memory 29 reprogrammed using an external programmer. Alternatively, the neurostimulator 12 can be programmed to automatically titrate therapy by up titrating the VNS through periodic incremental increases as described above. The titration process 1000 will continue until the ultimate therapeutic goal is reached.

Following the titration period, therapeutic VNS, as parametrically defined by the maintenance dose operating mode, is delivered to at least one of the vagus nerves. The stimulation system 11 delivers electrical therapeutic stimulation to the cervical vagus nerve of a patient 10 in a manner that results in creation and propagation (in both afferent and efferent directions) of action potentials within neuronal fibers of either the left or right vagus nerve independent of cardiac cycle.

In a further embodiment, the sensed heart rate data can be used to analyze therapeutic efficacy and patient condition. For instance, statistics could be determined from the sensed heart rate, either onboard by the neurostimulator 12 or by an external device, such as a programming computer following telemetric data retrieval. The sensed heart rate data statistics can include determining a minimum heart rate over a stated time period, a maximum heart rate over a stated time period, an average heart rate over a stated time period, and a variability of heart rate over a stated period, where the stated period could be a minute, hour, day, week, month, or other selected time interval. Still other uses of the heart rate sensor 31 and the sensed heart rate data are possible.

FIG. 11A is a simplified block diagram of an implanted neurostimulation system 1100 in accordance with embodiments of the present invention. The implanted neurostimulation system 1100 comprises a control system 1102 comprising a processor programmed to operate the system 1100, a memory 1103, a physiological sensor 1104, and a stimulation subsystem 1106. The physiological sensor 1104 may be configured to monitor any of a variety of patient physiological signals and the stimulation subsystem 1106 may be configured to deliver a stimulation signal to the patient. In one example, the physiological sensor 1104 comprises an ECG sensor for monitoring heart rate and the stimulation subsystem 1106 comprises a neurostimulator 12 programmed to deliver ON-OFF cycles of stimulation to the patient's vagus nerve.

The control system 1102 is programmed to activate the neurostimulator 12 to deliver varying stimulation intensities to the patient and to monitor the physiological signals in response to those stimulation signals.

The titration of the stimulation signal delivery and the monitoring of the patient's physiological response (e.g., heart rate) may be advantageously implemented using control system in communication with both the stimulation subsystem 1106 and the physiological sensor 1104, such as by incorporating all of these components into a single implantable device. In accordance with other embodiments, the control system may be implemented in a separate implanted device or in an external programmer 1120 or other external device, as shown in FIG. 11B. The external programmer 1120 in FIG. 11B may be utilized by a clinician or by the patient for adjusting stimulation parameters. The external programmer 1120 is in wireless communication with the implanted medical device 1110, which includes the stimulation subsystem 1116. In the illustrated embodiment, the physiological sensor 1114 is incorporated into the implanted medical device 1110, but in other embodiments, the sensor 1114 may be incorporated into a separate implanted device, may be provided externally and in communication with the external programmer 1120, or may be provided as part of the external programmer 1120.

It will be understood that the initial and target stimulation parameters described above are merely exemplary, and in other embodiments, different parameter levels may be used. In addition, although embodiments described above set the initial frequency and initial duty cycle at the target levels, in other embodiments, those initial parameters may also be set to levels below the target levels and gradually increased to achieve adequate adaptation.

In various embodiments described above, the patient's heart rate response is used as the patient parameter indicative of the desired physiological response. In other embodiments, different patient parameters may be monitored in conjunction with stimulation, including, for example, other heart rate variability parameters, ECG parameters such as PR interval and QT interval, and non-cardiac parameters such as respiratory rate, pupil diameter, and skin conductance. Increases and decreases in these patient parameters in response to changes in stimulation intensity may be used to identify the desired physiological response.

While the invention has been particularly shown and described as referenced to the embodiments thereof, those skilled in the art will understand that the foregoing and other changes in form and detail may be made therein without departing from the spirit and scope. For example, in various embodiments described above, the stimulation is applied to the vagus nerve. Alternatively, spinal cord stimulation (SCS) may be used in place of or in addition to vagus nerve stimulation for the above-described therapies. SCS may utilize stimulating electrodes implanted in the epidural space, an electrical pulse generator implanted in the lower abdominal area or gluteal region, and conducting wires coupling the stimulating electrodes to the generator.

Claims

1. A neurostimulation system, comprising:

an electrode assembly;
a neurostimulator coupled to the electrode assembly, the neurostimulator adapted to deliver a stimulation signal to a patient;
a physiological sensor configured to acquire a physiological signal from the patient; and
a processor coupled to the neurostimulator and the physiological sensor, the processor being configured to:
at an initial titration session, activate the neurostimulator to deliver the stimulation signal with an initial stimulation parameter set, the initial parameter set comprising an output current, a frequency, a pulse width, and a duty cycle;
perform a titration process, the titration process comprising:
increasing the output current of the stimulation signal until the stimulation signal comprises a target output current or adequate adaption is achieved, wherein adequate adaptation comprises at least one of a side effect level below a side effect tolerance zone boundary, a target physiological response or a target parameter set;
after increasing the output current of the stimulation signal, in response to the patient exceeding the side effect tolerance zone boundary before the stimulation signal comprises the target output current, decreasing the frequency and subsequently increasing the output current until either the stimulation signal comprises the target output current or the patient again exceeds the side effect tolerance zone boundary; and
after the stimulation signal comprises the target output current, increasing at least one of the frequency, the pulse width or the duty cycle while maintaining the target output current until a composite threshold is reached, wherein the composite threshold is reached when the stimulation signal comprises the target parameter set or the patient exceeds the side effect tolerance zone boundary.

2. The neurostimulation system of claim 1, wherein the target parameter set comprises a target frequency of between 8 Hz and 12 Hz.

3. The neurostimulation system of claim 1, wherein subsequently increasing the output current comprises maintaining the frequency, the pulse width and the duty cycle of the stimulation signal.

4. The neurostimulation system of claim 1, wherein decreasing the frequency and subsequently increasing the output current comprises decreasing the frequency to about 5 Hz or less.

5. The neurostimulation system of claim 1, wherein the titration process further comprises:

after decreasing the frequency to a lowered frequency level and subsequently increasing the output current, in response to the patient again exceeding the side effect tolerance zone boundary before the stimulation signal comprises the target output current while at the lowered frequency level, increasing the frequency to an elevated frequency level and subsequently increasing the duty cycle until either the stimulation signal comprises a target duty cycle or the patent subsequently exceeds the side effect tolerance zone boundary.

6. The neurostimulation system of claim 1, wherein decreasing the frequency and subsequently increasing the output current the further comprises after increasing the output current of the stimulation signal, in response to the patient exceeding the side effect tolerance zone boundary before the stimulation signal comprises the target output current, decreasing the frequency and the pulse width and subsequently increasing the output current until either the stimulation signal comprises the target output current or the patient again exceeds the side effect tolerance zone boundary.

7. The neurostimulation system of claim 1, wherein the processor is further configured to:

determine a physiological response to the stimulation signal by:
monitoring a baseline signal acquired by the physiological sensor during OFF time periods of the stimulation signal; and
monitoring a response signal acquired by the physiological sensor during ON time periods of the stimulation signal.

8. A neurostimulation system, comprising:

an electrode assembly;
a neurostimulator coupled to the electrode assembly, the neurostimulator adapted to deliver a stimulation signal to a patient;
a physiological sensor configured to acquire a physiological signal from the patient; and
a processor coupled to the neurostimulator and the physiological sensor, the processor configured to:
at an initial titration session, activate the neurostimulator to deliver the stimulation signal with an initial stimulation parameter set, the initial parameter set comprising an output current, a frequency, a pulse width, and a duty cycle;
perform a titration process, the titration process comprising:
increasing the output current of the stimulation signal until the stimulation signal comprises a target output current;
after increasing the output current of the stimulation signal, in response to the patient exceeding a side effect tolerance zone boundary before the stimulation signal comprises the target output current, decreasing the frequency and subsequently increasing the output current until either the stimulation signal comprises the target output current or the patient again exceeds the side effect tolerance zone boundary; and
after the stimulation signal comprises the target output current, increasing at least one of the frequency, the pulse width or the duty cycle while maintaining the target output current.

9. The neurostimulation system of claim 8, wherein subsequently increasing the output current comprises maintaining the frequency, the pulse width and the duty cycle of the stimulation signal.

10. The neurostimulation system of claim 8, wherein decreasing the frequency and subsequently increasing the output current comprises decreasing the frequency to about 5 Hz or less.

11. The neurostimulation system of claim 8, wherein the titration process further comprises:

after decreasing the frequency to a lowered frequency level and subsequently increasing the output current, in response to the patient again exceeding the side effect tolerance zone boundary before the stimulation signal comprises the target output current while at the lowered frequency level, increasing the frequency to an elevated frequency level and subsequently increasing the duty cycle until either the stimulation signal comprises a target duty cycle or the patent subsequently exceeds the side effect tolerance zone boundary.

12. The neurostimulation system of claim 8, wherein decreasing the frequency and subsequently increasing the output current further comprises after increasing the output current of the stimulation signal, in response to the patient exceeding the side effect tolerance zone boundary before the stimulation signal comprises the target output current, decreasing the frequency and the pulse width and subsequently increasing the output current until either the stimulation signal comprises the target output current or the patient again exceeds the side effect tolerance zone boundary.

13. The neurostimulation system of claim 8, wherein the processor is further configured to:

determine a physiological response to the stimulation signal by:
monitoring a baseline signal acquired by the physiological sensor during OFF time periods of the stimulation signal; and
monitoring a response signal acquired by the physiological sensor during ON time periods of the stimulation signal.
Referenced Cited
U.S. Patent Documents
5330507 July 19, 1994 Schwartz
5522854 June 4, 1996 Ideker et al.
5707400 January 13, 1998 Terry, Jr. et al.
5928272 July 27, 1999 Adkins et al.
5978709 November 2, 1999 Begemann et al.
6006134 December 21, 1999 Hill et al.
6266564 July 24, 2001 Hill et al.
6354991 March 12, 2002 Gross et al.
6449507 September 10, 2002 Hill et al.
6473644 October 29, 2002 Terry et al.
6508771 January 21, 2003 Padmanabhan et al.
6522926 February 18, 2003 Kieval et al.
6600954 July 29, 2003 Cohen et al.
6610713 August 26, 2003 Tracey
6616624 September 9, 2003 Kieval
6622041 September 16, 2003 Terry, Jr. et al.
6652449 November 25, 2003 Gross et al.
6684105 January 27, 2004 Cohen et al.
6690971 February 10, 2004 Schauerte et al.
6712772 March 30, 2004 Cohen et al.
6718208 April 6, 2004 Hill et al.
6838471 January 4, 2005 Tracey
6839594 January 4, 2005 Cohen et al.
6850801 February 1, 2005 Kieval et al.
6862480 March 1, 2005 Cohen et al.
6892098 May 10, 2005 Ayal et al.
6896651 May 24, 2005 Gross et al.
6904318 June 7, 2005 Hill et al.
6907295 June 14, 2005 Gross et al.
6963773 November 8, 2005 Waltman et al.
6963779 November 8, 2005 Shankar
6985774 January 10, 2006 Kieval et al.
7010345 March 7, 2006 Hill et al.
7072720 July 4, 2006 Puskas
7123961 October 17, 2006 Kroll et al.
7139607 November 21, 2006 Shelchuk
7158832 January 2, 2007 Kieval et al.
7184828 February 27, 2007 Hill et al.
7184829 February 27, 2007 Hill et al.
7218964 May 15, 2007 Hill et al.
7221979 May 22, 2007 Zhou et al.
7225017 May 29, 2007 Shelchuk
7225019 May 29, 2007 Jahns et al.
7237320 July 3, 2007 Lam
7245967 July 17, 2007 Shelchuk
7260431 August 21, 2007 Libbus et al.
7269457 September 11, 2007 Shafer et al.
7277761 October 2, 2007 Shelchuk
7295881 November 13, 2007 Cohen et al.
7305265 December 4, 2007 Fukui
7321793 January 22, 2008 Ezra et al.
7324853 January 29, 2008 Ayal et al.
7336997 February 26, 2008 Fukui
7346398 March 18, 2008 Gross et al.
7387603 June 17, 2008 Gross et al.
7389149 June 17, 2008 Rossing et al.
7395119 July 1, 2008 Hagen et al.
7403819 July 22, 2008 Shelchuk et al.
7418292 August 26, 2008 Shafer
7452800 November 18, 2008 Sosnowchik et al.
7480532 January 20, 2009 Kieval et al.
7481759 January 27, 2009 Whitehurst et al.
7485104 February 3, 2009 Kieval
7493167 February 17, 2009 Hussein et al.
7499742 March 3, 2009 Bolea et al.
7499747 March 3, 2009 Kieval et al.
7499748 March 3, 2009 Moffitt et al.
7502650 March 10, 2009 Kieval
7542800 June 2, 2009 Libbus et al.
7548780 June 16, 2009 Libbus et al.
7551958 June 23, 2009 Libbus et al.
7561922 July 14, 2009 Cohen et al.
7561923 July 14, 2009 Libbus et al.
7570999 August 4, 2009 Libbus et al.
7582053 September 1, 2009 Gross et al.
7584004 September 1, 2009 Caparso et al.
7587238 September 8, 2009 Moffitt et al.
7606622 October 20, 2009 Reeve
7613511 November 3, 2009 Wu et al.
7613516 November 3, 2009 Cohen et al.
7616990 November 10, 2009 Chavan et al.
7617003 November 10, 2009 Caparso et al.
7623926 November 24, 2009 Rossing et al.
7627384 December 1, 2009 Ayal et al.
7628750 December 8, 2009 Cohen et al.
7630760 December 8, 2009 Libbus et al.
7634315 December 15, 2009 Cholette
7634317 December 15, 2009 Ben-David et al.
7640057 December 29, 2009 Libbus et al.
7647101 January 12, 2010 Libbus et al.
7647114 January 12, 2010 Libbus
7650190 January 19, 2010 Zhou et al.
7657312 February 2, 2010 Pastore et al.
7660628 February 9, 2010 Libbus et al.
7664548 February 16, 2010 Amurthur et al.
7668602 February 23, 2010 Ben-David et al.
7672733 March 2, 2010 Zhou et al.
7676275 March 9, 2010 Farazi et al.
7684866 March 23, 2010 Fowler et al.
7689286 March 30, 2010 Pastore et al.
7711415 May 4, 2010 Farazi et al.
7711421 May 4, 2010 Shafer et al.
7734355 June 8, 2010 Cohen et al.
7751884 July 6, 2010 Ternes et al.
7769442 August 3, 2010 Shafer
7769446 August 3, 2010 Moffitt et al.
7778702 August 17, 2010 Ben-David et al.
7778703 August 17, 2010 Gross et al.
7778711 August 17, 2010 Ben-David et al.
7783353 August 24, 2010 Libbus et al.
7797041 September 14, 2010 Libbus et al.
7801603 September 21, 2010 Westlund et al.
7801604 September 21, 2010 Brockway et al.
7801614 September 21, 2010 Rossing et al.
7805193 September 28, 2010 Libbus et al.
7805203 September 28, 2010 Ben-David et al.
7813805 October 12, 2010 Farazi
7813812 October 12, 2010 Kieval et al.
7835797 November 16, 2010 Rossing et al.
7840266 November 23, 2010 Libbus et al.
7840271 November 23, 2010 Kieval et al.
7844346 November 30, 2010 Cohen et al.
7848812 December 7, 2010 Crowley et al.
7848816 December 7, 2010 Wenzel et al.
7869869 January 11, 2011 Farazi
7885709 February 8, 2011 Ben-David
7885711 February 8, 2011 Ben-Ezra et al.
7890185 February 15, 2011 Cohen et al.
7894907 February 22, 2011 Cowan et al.
7904151 March 8, 2011 Ben-David et al.
7904175 March 8, 2011 Scott et al.
7904176 March 8, 2011 Ben-Ezra et al.
7908008 March 15, 2011 Ben-David et al.
7916013 March 29, 2011 Stevenson
7925342 April 12, 2011 Amurthur et al.
7925352 April 12, 2011 Stack et al.
7974693 July 5, 2011 Ben-David et al.
8005542 August 23, 2011 Ben-Ezra et al.
8005545 August 23, 2011 Ben-David et al.
8036745 October 11, 2011 Ben-David et al.
8060197 November 15, 2011 Ben-David et al.
8065021 November 22, 2011 Gross et al.
8083663 December 27, 2011 Gross et al.
8116881 February 14, 2012 Cohen et al.
8131362 March 6, 2012 Moffitt et al.
8160701 April 17, 2012 Zhao et al.
8160705 April 17, 2012 Stevenson et al.
8195290 June 5, 2012 Brockway et al.
8224436 July 17, 2012 Libbus et al.
8249711 August 21, 2012 Libbus et al.
8369943 February 5, 2013 Shuros et al.
8386038 February 26, 2013 Bianchi et al.
8401640 March 19, 2013 Zhao et al.
8417354 April 9, 2013 Zhang et al.
8571654 October 29, 2013 Libbus et al.
8577458 November 5, 2013 Libbus et al.
8600505 December 3, 2013 Libbus et al.
8634921 January 21, 2014 Chavan et al.
8688212 April 1, 2014 Libbus et al.
8918190 December 23, 2014 Libbus et al.
9533153 January 3, 2017 Libbus
20020107553 August 8, 2002 Hill et al.
20030040774 February 27, 2003 Terry et al.
20030171781 September 11, 2003 Florio et al.
20040199210 October 7, 2004 Shelchuk
20050049655 March 3, 2005 Boveja et al.
20050065553 March 24, 2005 Ezra et al.
20050125044 June 9, 2005 Tracey
20050131467 June 16, 2005 Boveja
20050267542 December 1, 2005 David et al.
20060015153 January 19, 2006 Gliner et al.
20060100668 May 11, 2006 Ben-David et al.
20060190053 August 24, 2006 Dobak, III
20060206155 September 14, 2006 Ben-David et al.
20060253161 November 9, 2006 Libbus et al.
20070067004 March 22, 2007 Boveja et al.
20070093870 April 26, 2007 Maschino
20070213773 September 13, 2007 Hill et al.
20070233194 October 4, 2007 Craig
20070255320 November 1, 2007 Inman et al.
20070276453 November 29, 2007 Hill et al.
20080021503 January 24, 2008 Whitehurst et al.
20080033511 February 7, 2008 Dobak
20080058874 March 6, 2008 Westlund et al.
20080132983 June 5, 2008 Cohen et al.
20080147140 June 19, 2008 Ternes et al.
20080183258 July 31, 2008 Inman
20080243196 October 2, 2008 Libbus et al.
20080319513 December 25, 2008 Pu et al.
20090030493 January 29, 2009 Colborn et al.
20090118777 May 7, 2009 Iki et al.
20090124848 May 14, 2009 Miazga
20090149900 June 11, 2009 Moffitt et al.
20090248097 October 1, 2009 Tracey et al.
20090270953 October 29, 2009 Ecker et al.
20100010556 January 14, 2010 Zhao et al.
20100010603 January 14, 2010 Ben-David et al.
20100016919 January 21, 2010 Hill et al.
20100042173 February 18, 2010 Farazi et al.
20100114197 May 6, 2010 Burnes et al.
20100174341 July 8, 2010 Bolea et al.
20100286740 November 11, 2010 Libbus et al.
20100331908 December 30, 2010 Farazi
20110015692 January 20, 2011 Libbus et al.
20110082514 April 7, 2011 Libbus et al.
20110098796 April 28, 2011 Ben-David et al.
20110224749 September 15, 2011 Ben-David et al.
20110257708 October 20, 2011 Kramer et al.
20110313488 December 22, 2011 Hincapie Ordonez et al.
20120143286 June 7, 2012 Hahn et al.
20120172742 July 5, 2012 Arcot-Krishnamurthy et al.
20120185007 July 19, 2012 Ziegler et al.
20120185010 July 19, 2012 Zhou et al.
20120192874 August 2, 2012 Bolea et al.
20120271374 October 25, 2012 Nelson et al.
20120303080 November 29, 2012 Ben-David et al.
20130053926 February 28, 2013 Hincapie Ordonez et al.
20130158616 June 20, 2013 Libbus et al.
20130158617 June 20, 2013 Libbus et al.
20130158618 June 20, 2013 Libbus et al.
20130238047 September 12, 2013 Libbus et al.
20130289646 October 31, 2013 Libbus et al.
20140025132 January 23, 2014 Libbus et al.
20140135862 May 15, 2014 Libbus et al.
20140135863 May 15, 2014 Libbus et al.
20140135864 May 15, 2014 Libbus et al.
20140188191 July 3, 2014 Libbus et al.
20140228905 August 14, 2014 Bolea
20140277232 September 18, 2014 Libbus et al.
20150094962 April 2, 2015 Hoegh et al.
Foreign Patent Documents
WO-2011/159527 December 2011 WO
WO-2013/086175 June 2013 WO
Other references
  • US 8,315,702, 11/2012, Chavan et al. (withdrawn)
  • Zhang, et al., “Chronic Vagus Nerve Stimulation Improves Autonomic Control and Attenuates Systemic Inflammation and Heart Failure Progression in a Canine High-Rate Pacing Model,” Journal of the American Heart Association, Circ Heart Fail, 2, pp. 692-699 (2009).
  • Abraham, et al., “Devices in the management of advanced, chronic heart failure,” Nature Reviews, vol. 10, pp. 98-110 (Feb. 2013) (Published online Dec. 11, 2012).
  • Adamson, et al., “Continuous Autonomic Assessment in Patients with Symptomatic Heart Failure: Prognostic Value of Heart Rate Variability Measured by an Implanted Cardiac Resynchronization Device,” Circulation, Journal of the American Heart Association, 110, pp. 2389-2394 (2004).
  • Agostoni, et al., “Functional and Histological Studies of the Vagus Nerve and its Branches to the Heart, Lungs and Abdominal Viscera in the Cat,” J. Physiol. 135, pp. 182-205 (1957).
  • Ajani, et al., “Prevalence of High C-Reactive Protein in Persons with Serum Lipid Concentrations within Recommended Values,” Chemical Chemistry, 50:9, pp. 1618-1622 (2004).
  • Akiyama, et al., “Effects of right and left vagal stimulation on left ventricular acetylcholine levels in the cat,” Acta Physiol Scand, 172, pp. 11-16 (2001).
  • Anand, et al., “C-Reactive Protein in Heart Failure: Prognostic Value and the Effect of Valsartan,” Circulation, Journal of the American Heart Association, 112, pp. 1428-1434 (2005).
  • Anholt, et al., “Recruitment and blocking properties of the CardioFit stimulation lead,” Journal of Neural Engineering, 8, pp. 1-6, (2011).
  • Ardell, et al.; “Selective vagal innervation of sinoatrial and atrioventricular nodes in canine heart,” Am. J. Physiol. 251 (Heart Circ. Physiol. 20), pp. H764-H773 (1986).
  • Armour, “Cardiac neuronal hierarchy in health and disease,” Am J Physiol Regul Integr Comp Physiol, 287, pp. R262-R271 (2004).
  • Armour, “Myocardial ischaemia and the cardiac nervous system,” Cardiovascular Research, 41, pp. 41-54 (1999).
  • Armour, “The little brain on the heart,” Cleveland Clinic Journal of Medicine, vol. 74, supp. 1, pp. S48-S51 (Feb. 2007).
  • Armour, et al., “Functional anatomy of canine cardiac nerves,” Acta anat., 91, pp. 510-528 (1975).
  • Armour, et al., “Localized myocardial responses to stimulation of small cardiac branches of the vagus,” American Journal of Physiology, vol. 228, No. 1 pp. 141-148 (Jan. 1975).
  • Armour, JA, “Potential clinical relevance of the ‘little brain’ on the mammalian heart,” Experimental Physiology, vol. 1 93, No. 2, pp. 165-176 (Feb. 2008). Online Publication Date: Nov. 2, 2007. Available at: http://ep.physoc.org/content/93/2/165.long.
  • Asala, et al., “An electron microscope study of vagus nerve composition in the ferret,” Anat Embryol, 175, pp. 247-253 (1986).
  • Aukrust, et al., “Inflammatory and anti-inflammatory cytokines in chronic heart failure: Potential therapeutic implications,” Annals of Medicine, 37, pp. 74-85 (2005).
  • Author Unknown, “Nerve fiber—Types and Function,” www.boddunan.com Available at www.boddunan.com/education/20-medicine-a-surgery/12730-nerver-fiber-types-and-function.html (Apr. 19, 2010).
  • Author Unknown, American Diabetes Association, “Standards of Medical Care in Diabetes—2012,” Diabetes Care, vol. 35, supplement 1, pp. S11-S63 (Jan. 2012).
  • Author Unknown, Staff of Adinstruments, “Principles of Nerve Stimulation,” Application Note, ADInstruments (Apr. 2002).
  • Bae, et al., “Gliosis in the Amygdala Following Myocardial Infarction in the Rat,” J Vet Med Sci, 72(8), pp. 1041-1045 (2010).
  • Bernik, et al., “Pharmacological Stimulation of the Cholinergic Antiinflammatory Pathway,” J. Exp. Med, vol. 195, No. 6, pp. 781-788 (Mar. 18, 2002).
  • Berthoud, et al., “Functional and chemical anatomy of the afferent vagal system,” Autonomic Neuroscience: Basic and Clinical, 85, pp. 1-17 (2000).
  • Bhagat, et al., “Differential Effect of Right and Left Vagal Stimulation on Right and Left Circumflex Coronary Arteries,” S A Medical Journal, 50, pp. 1591-1594 (1976).
  • Biasucci, et al., “Elevated Levels of C-Reactive Protein at Discharge in Patients with Unstable Angina Predict Recurrent Instability,” Circulation, Journal of the American Heart Association, 99, pp. 855-860 (1999).
  • Bibevski, et al., “Evidence for impaired vagus nerve activity in heart failure,” Heart Fail Rev, 16, pp. 129-135 (2011).
  • Bibevski, et al., “Ganglionic Mechanisms Contribute to Diminished Vagal Control in Heart Failure,” Circulation, Journal of the American Heart Association, 99, pp. 2958-2963 (1999).
  • Bilgutay, et al., “Vagal Tuning A new concept in the treatment of supraventricular arrhythmias, angina pectoris, and heart failure,” Journal of Thoracic and Cardiovascular Surgery, vol. 56, No. 1, pp. 71-82 (Jul. 1968).
  • Binkley, et al., “Parasympathetic Withdrawal is an Integral Component of Autonomic Imbalance in Congestive Heart Failure: Demonstration in Human Subjects and Verification in a Paced Canine Model of Ventricular Failure,” JACC, vol. 18, No. 2, pp. 464-472 (Aug. 1991).
  • Bois, et al., “Mode of action of bradycardic agent, S 16257, on ionic currents of rabbit sinoatrial node cells,” Abstract, British Journal of Pharmacology, 118(4):1051-7 (1996).
  • Bonaz, et al., “Vagus nerve stimulation: From epilepsy to the cholinergic anti-inflammatory pathway,” Neurogastroenterology & Motility, pp. 1-14 (2013).
  • Borggrefe, et al., “Vagal Stimulation Devices,” ESC Congress 2010 (2010).
  • Borovilkova, et al., “Vagus nerve stimulation attenuates the systemic inflammatory response to endotoxin,” Nature, vol. 405, pp. 458-462 (May 25, 2000).
  • Brack, et al., “Mechanisms underlying the autonomic modulation of ventricular fibrillation initiation—tentative prophylactic properties in vagus nerve stimulation on malignant arrhythmias in heart failure,” Heart Fail Rev (Published online Jun. 8, 2012).
  • Bronzing, “Biomedical Engineering Fundamentals,” CRC Press, Chapter 30, pp. 30-10-30-15 (Apr. 2006).
  • Buschman, et al., “Heart Rate Control Via Vagus Nerve Stimulation,” Neuromodulation, vol. 9, No. 3, pp. 214-220 (2006).
  • Butterwick, et al., “Tissue Damage by Pulsed Electrical Stimulation,” IEEE Transactions on Biomedical Engineering, vol. 54, No. 12, pp. 2261-2267 (Dec. 2007).
  • Calkins, et al., “Comparison of Responses to Isoproterenol and Epinephrine During Head-Up Tilt in Suspected Vasodepressor Syncope,” The American Journal of Cardiology, vol. 67 pp. 207-209 (Jan. 15, 1991).
  • Castoro et al., “Excitation properties of the right cervical vagus nerve in adult dogs,” Experimental Neurology, vol. 2 227, iss. 1, pp. 62-68 (Jan. 2011). Online Publication Date: Sep. 17, 2010. Available at: http://www.sciencedirecl.com/science/article/pii/SOO1448861000347X.
  • Chapleau, et al., “Methods of assessing vagus nerve activity and reflexes,” Heart Fail Rev, 16, pp. 109-127 (2011).
  • Chen, et al., “National and Regional Trends in Heart Failure Hospitalization and Mortality Rates for Medicare Beneficiaries, 1998-2008,” JAMA, vol. 306, No. 15 (Oct. 19, 2011).
  • Chen, et al., “Role of Atrial Electrophysiology and Autonomic Nervous System in Patients with Supraventricular Tachycardia and Paroxysmal Artrial Fibrillation,” J Am Coll Cardiol, vol. 32, No. 3, pp. 732-738 (Sep. 1998).
  • Cheng, et al., “Long-term Outcomes in Individuals with Prolonged PR Interval or First-Degree Atrioventricular Block,” JAMA, vol. 301, No. 24 pp. 2571-2577 (Jun. 24, 2009).
  • Chiou, et al., “Effects of Continuous Enhanced Vagal Tone and Dual Atrioventricular Node and Accessory Pathways,” Circulation, Journal of the American Heart Association, 107, pp. 2583-2588 (2003).
  • Cohen, et al., “Histopathology of the stimulated Vagus nerve: Primum non nocere,” Heart Fail Rev, 16, pp. 163-169 (2011).
  • Colombo, et al., “Comparison between spectral analysis and the phenylephrine methods for the assessment of baroreflex sensitivity in chronic heart failure,” Clinical Science, 97, pp. 503-513 (1999).
  • Cryan, et al., “Animal models and mood disorders: recent developments,” Current Opinion in Psychiatry, 20, pp. 1-7 (2007).
  • Das, “Vagal nerve stimulation in prevention and management of coronary heart disease,” World J. Cardiol, 3(4), pp. 105-110 (Apr. 26, 2011).
  • De Castro, et al., “Parasympathetic-mediated atrial fibrillation during tilt test associated with increased baroreflex sensitivity,” The European Society of Cardiology, Europace, 8, pp. 349-351 (2006).
  • De Ferrari et al., Chronic Vagus Nerve Stimulation: A New and Promising Therapeutic Approach for Chronic Heart Failure, European Heart Journal, vol. 32, Oct. 28, 2010, pp. 847-855.
  • De Ferrari, et al., “Baroreflex Sensitivity Predicts Long-Term Cardiovascular Mortality After Myocardial Infarction Even in Patients with Preserved Left Ventricular Function,” Journal of the American College of Cardiology, vol. 50, No. 24, pp. 2285-2290 (2007).
  • De Ferrari, et al., “Chronic Vagal Stimulation in Patients with Congestive Heart Failure,” 31st Annual International Conference of the IEE EMBS (2009).
  • De Ferrari, et al., “Vagus nerve stimulation: from pre-clinical to clinical application: challenges and future directions,” Heart Fail Rev, 16, pp. 195-203 (2011) (Published Online Dec. 17, 2010).
  • De Jonge, et al., “Stimulation of the vagus nerve attenuates macrophage activation by activating the Jak2-STAT3 signaling pathway,” Nature Immunology, vol. 6, No. 8, pp. 844-852 (Aug. 2005).
  • Desai, et al., “Pharmacologic modulation of parasympathetic activity in heart failure,” Heart Fail Rev, 16, pp. 179-193 (Published online: Oct. 6, 2010) (2011).
  • Dickerson, et al., “Parasympathetic neurons in the cranial medial ventricular fat pad on the dog heart selectively decrease ventricular contractility,” Journal of the Autonomic Nervous System, 70, pp. 129-141 (1998).
  • Dunlap, et al., “Mechanisms of altered vagal control in heart failure: influence of muscarinic receptors and acetyicholinesterase activity,” Am J Physiol Heart Circ Physiol, 285, pp. H1632-H1640 (Jun. 26, 2003).
  • Elsenbruch, et al., “Heart Rate Variability During Waking and Sleep in Healthy Males and Females,” Sleep, vol. 22, No. 8, pp. 1067-1071 (1999).
  • Euler, et al., “Acetylcholine release by a stimulus train lowers atrial fibrillation threshold,” Am. J Physiol. 253 (Heart Gire. Physiol, 22), pp. H863-H868 (1987).
  • Evans, et al., “Histological and functional studies on the fibre composition of the vagus nerve of the rabbit,” Journal of Anatomy, 130, pp. 139-151 (1954).
  • Fallen, “Vagal Afferent Stimulation as a Cardioprotective Strategy? Introducing the Concept,” A.N.E., vol. 10, No. 4 (Oct. 2005).
  • Fan, et al., “Transvenous vagus nerve stimulation: A potential heart failure therapy is feasible in humans,” JACC, vol. 55, issue 10A, pp. E152-E153 (2010).
  • Fazan, et al., “Diabetic Peripheral Neuropathies: A Morphometric Overview,” Int. J. Morphol, 28(1), pp. 51-64 (2010).
  • Feinauer, et al., “Ouabain enhances release of acetylcholine in the heart evoked by unilateral vagal stimulation,” Arch Pharmacol, 333, pp. 7-12 (1986).
  • Fonarow, et al., “Incremental Reduction in Risk of Death Associated with Use of Guideline-Recommended Therapies in Patients with Heart Failure: A Nested Case-Control Analysis of Improve HF,” J Am Heart Assoc, 1, pp. 16-26 (2012).
  • Ford, et al., “The effects of electrical stimulation of myelinated and non-myelinated vagal fibres on heart rate in the rabbit,” J. Physiol. 380, pp. 341-347 (1986).
  • Furukawa, et al., “Effects of Verapamil, Zatebradine, and E-4031 on the Pacemaker Location and Rate in Response to Sympathetic Stimulation in Dog Hearts,” The Journal of Pharmacology and Experimental Therapeutids, vol. 289, No. 3, pp. 1334-1342 (1999).
  • Furukawa, et al., “Selective inhibition by zatebradine and discrete parasympathetic stimulation of the positive chronotropic response to sympathetic stimulation in anesthetized dogs,” Abstract, Journal of Pharmacology & Experimental Therapeutics, 272(2):744-9 (1995).
  • Gatti, et al., “Can neurons in the nucleus ambiguous selectively regulate cardiac rate and atrioventricular conduction?” Journal of the Autonomic Nervous System, 57, pp. 123-127 (1996).
  • Gatti, et al., “Vagal control of left ventricular contractility is selectively mediated by a cranioventricular intracardiac ganglion in the cat,” Journal of the Autonomic Nervous System, 66, pp. 138-144 (1997).
  • Gibbons, et al., “Neuromodulation targets intrinsic cardiac neurons to attenuate neuronally mediated atrial arrhythmias,” Am J Physiol Regul Integr Comp Physiol 302: R357-R364 (2012) (First published Nov. 16, 2011).
  • Gottdiener, et al., “Predictors of Congestive Heart Failure in the Elderly: The Cardiovascular Health Study,” Journal of the American College of Cardiology, vol. 35, No. 6, pp. 1628-1637 (2000).
  • Gray, et al., “Parasympathetic control of the Heart. II. A novel interganglionic intrinsic cardiac circuit mediates neural control of heart rate,” J. Appl Physiol, 96, pp. 2273-2278 (2004).
  • Gray, et al., “Parasympathetic control of the Heart. III. Neuropeptide Y-immunoreactive nerve terminals synapse on three populations of negative chronotropic vagal preganglionic neurons,” J. Appl Physiol, 96, pp. 2279-2287 (2004).
  • Grill, “Chapter 14—Principles of Electric Field Generation for Stimulation of the Central Nervous System,” Neuromodulation, Academic Press (2009).
  • Guilleminault, et al., “Cyclical Variation of the Heart Rate in Sleep Apnea Syndrome,” The Lancet, pp. 126-131 (Jan. 21, 1984).
  • Hardwick, et al., “Chronic myocardial infarction induces phenotypic and functional remodeling in the guinea pig cardiac plexus,” Am J Physiol Regulatory Integrative Comp Physiol, 295, pp. 1926-1933 (2008).
  • Hardwick, et al., “Remodeling of the guinea pig intrinsic cardiac plexus with chronic pressure overload,” Am J Physiol Regulatory Integrative Comp Physiol, 297, pp. 859-866 (2009).
  • Hauptman, et al., “The vagus nerve and autonomic imbalance in heart failure: past, present, and future,” Heart Fail Rev, 16, pp. 97-99 (2011).
  • Hellyer, et al., “Autonomic nerve activity and blood pressure in ambulatory dogs,” Heart Rhythym, vol. 11(2), pp. 307-313 (Feb. 2014).
  • Hirooka, et al., “Imbalance of central nitric oxide and reactive oxygen species in the regulation of sympathetic activity and neural mechanisms of hypertension,” Am J Physiol Regulatory Integration Comp Physiol, 300, pp. 818-826 (2011).
  • Hoffman, et al., “Vagus Nerve Components,” Anat Rec, 127, pp. 551-568 (1957).
  • Hu, et al., “Role of sympathetic nervous system in myocardial ischemia injury: Beneficial or deleterious?” Letters to the Editor, Elsevier Ireland Ltd. (Mar. 27, 2012).
  • Hua, et al., “Left vagal stimulation induces dynorphin release and suppresses substance P release from the rat thoracic spinal cord during cardiac ischemia,” Am J Physiol Regulatory Integration Comp Physiol, 287, pp. 1468-1477 (2004).
  • Huston, et al., “Splenectomy inactivates the cholinergic antiinflammatory pathway during lethal endotoxemia and polymicrobial sepsis,” J. Exp. Med, vol. 203, No. 7 pp. 1623-1628 (Jun. 19, 2006).
  • Huston, et al., “Transcutaneous vagus nerve stimulation reduces serum high mobility group box 1 levels and improves survival in murine sepsis,” Grit Care Med, vol. 35, No. 12, pp. 2762-2768 (2007).
  • Ingemansson, et al., “Autonomic modulation of the atrial cycle length by the head up tilt test: non-invasive evaluation in patients with chronic atrial fibrillation,” Heart, 80, pp. 71-76 (1998).
  • International Search Report for PCT Patent Application No. PCT/US2015/043878, dated Oct. 29, 2015, 6 pages.
  • Ito, et al., “Efferent sympathetic and vagal innervation of the canine right ventricle,” Circulation, Journal of the American Heart Association, vol. 90, pp. 469-1468 (1994).
  • Jacques, et al., “Spinal Cord Stimulation Causes Potentiation of Right Vagus Nerve Effects on Atrial Chronotropic Function and Repolarization in Canines,” Journal of Cardiovascular Electrophysiology, vol. 22, No. 4, pp. 440-447 (Apr. 2011).
  • Jaenisch, et al., “Respiratory muscle training improves baroreceptor sensitivity, decrease sympathetic tonus and increase vagal effect in rats with heart failure,” European Heart Journal, 32 (Abstract Supplement, pp. 976 (2011).
  • Jammes, et al., “Afferent and efferent components of the bronchial vagal branches in cats,” Journal of the Autonomic Nervous System, 5, pp. 165-176 (1982).
  • Janabi, et al., “Oxidized LDL-Induced NF-kB Activation and Subsequent Expression of Proinflammatory Genes are Defective in Monocyte-Derived Macrophages from CD36-Deficient Patients,” Arterioscler Thromb Vase Biol., 20:1953-1960 (2000).
  • Janse, et al., “Effects of unilateral stellate ganglion stimulation and ablation on electrophysiologic changes induced by acute myocardial ischemia in dogs,” Circulation, Journal of the American Heart Association, 72, pp. 585-595 (1985).
  • Jessup; et al., “2009 Focused Update: ACCF/AHA Guidelines for the Diagnosis and Management of Heart Failure in Adults,” Circulation, Journal of the American Heart Association, vol. 119, pp. 1977-2016 (2009).
  • Johnson, et al., “Parasympathetic control of the heart. I. An interventriculo-septal ganglion is the major source of the vagal intracardiac innervation of the ventricles,” J Appl Physiol, 96, pp. 2265-2272 (2004).
  • Kakinuma, et al., “Cholinoceptive and cholinergic properties of cardiomyocytes involving an amplification mechanism for vagal efferent effects in sparsely innervated ventricular myocardium,” FEBS Journal, 276, pp. 5111-5125 (2009).
  • Kalman, “Specific effects of zatebradine on sinus node function: suppression of automaticity, prolongation of sinoatrial conduction and pacemaker shift in the denervated canine heart,” Abstract, Journal of Pharmacology & Experimental Therapeutics, 272(1):85-93 (1995).
  • Kaneko, et al., “C-Reactive Protein in Dilated Cardiomyopathy,” Cardiology, 91, pp. 215-219 (1999).
  • Katare, et al., “Vagal nerve stimulation prevents reperfusion injury through inhibition of opening of mitochondrial permeability transition pore independent of bradycardiac effect,” The Journal of Thoracic and Cardiovascular Surgery, vol. 137, No. 1, pp. 223-231 (2009).
  • Katz, et al., “Diseases of the heart in the Works of Hippocrates,” Br Heart J, 24, pp. 257-264 (1962).
  • Kawada, et al., “High-frequency dominant depression of peripheral vagal control of heart rate in rats with chronic heart failure,” Acta Physiol 207, 494-502 (2013).
  • Kawada, et al., “Vagal stimulation suppresses isschemia-induced myocardial interstitial norepinephrine release,” Life Sciences, 78, pp. 882-887 (2006).
  • Kawashima, “The autonomic nervous system of the human heart with special reference to its origin, course, and peripheral distribution,” Anat Embryol, 209, pp. 425-438 (2005).
  • Klein et al., “Vagus nerve stimulation: A new approach to reduce heart failure,” Cardiology Journal, vol. 17, iss. 6, pp. 638-643 (2010).
  • Kliks, et al., “Influence of Sympathetic Tone on Ventricular Fibrillation Threshold During Experimental Coronary Occlusion,” The American Journal of Cardiology, vol. 36, pp. 45-49 (Jul. 1975).
  • Kolman, et al., “The effect of vagus nerve stimulation upon vulnerability of the canine ventricle: role of sympathetic-parasympathetic interactions,” Journal of the American Heart Association, 52, pp. 578-585 (1975).
  • Kong, et al., “Optimizing the Parameters of Vagus Nerve Stimulation by Uniform Design in Rats with Acute Myocardial Infarction,” PLOS One, vol. 7, issue 11 (Nov. 2012).
  • Koopman, et al., “Pilot study of stimulation of the cholinergic anti-inflammatory pathway with an implantable vagus nerve stimulation device in patients with rheumatoid arthritis,” Abstract (2012).
  • Kulbertus, et al., ed., “Neurocardiology,” Futura Publishing Co., pp. 13 (“Anatomy of the Cardiac Efferent Innvervation”); 61-63 (“Autonomic Neural Control”); 87, 89, 92¬93 (“Sympathetic-Parasympathetic Interactions”); 183, 187 (“Parasympathetic Nervous System”); 104 (1988).
  • La Rovere, et al., “Baroreflex Sensitivity and Heart Rate Variability in the Identification of Patients at Risk for Life-Threatening Arrhythmias: Implications for Clinical Trials,” Circulation, Journal of the American Heart Association, 103, pp. 2072-2077 (2001).
  • La Rovere, et al., “Baroreflex sensitivity and heart-rate variability in prediction of total cardiac mortality after myocardial infarction. ATRAMI (Autonomic Tone and Reflexes After Myocardial Infarction) Investigators,” Lancet, 351(9101), pp. 478-484 (Feb. 14, 1998).
  • Lane, et al., “Prediction and Prevention of Sudden Cardiac Death in Heart Failure,” Heart, 91, pp. 674-680 (2005).
  • Lechat, et al., “Heart rate and Cardiac Rhythm Relationships with Bisoprolol Benefit in Chronic Heart Failure in CIBIS II Trial,” Circulation, Journal of American Heart Association, 103, pp. 1428-1433 (2001).
  • Lewis, et al., “Vagus nerve stimulation decreases left ventricular contractility in vivo in the human and pig heart,” Journal of Physiology, 534, pp. 547-552 (2001).
  • Li et al., “Vagal Nerve Stimulation Markedly Improves Long-Term Survival After Chronic Heart Failure in Rats,” Circulation: Journal of the American Heart Association, vol. 109, iss. 1, pp. 120-124 (Jan. 2004). Online publication date: Dec. 8, 2003.
  • Li, et al., “Early vagal stimulation markedly prevented cardiac dysfunction in rats after acute myocardial infarction in addition to suppressing arrhythmic death,” European Heart Journal, 32 (Abstract Supplement), pp. 297-298 (2011).
  • Li, et al., “Inflammatory cytokines and nitric oxide in heart failure and potential modulation by vagus nerve stimulation,” Heart Fail Rev, 16, pp. 137-145 (2011).
  • Li, et al., “Low-Level Vagosympathetic Stimulation. A Paradox and Potential New Modality for the Treatment of Focal Atrial Fibrillation,” Gire Arrhythm Electrophysiol, Journal of American Heart Association, 2, pp. 645-651 (2009).
  • Li, et al., “Restoration of vagal tone by donepezil, on top of losartan treatment, markedly suppresses ventricular dysfunction and improves long-term survival in chronic heart failure rats,” European Heart Journal, 32 (Abstract Supplement), pp. 642 (2011).
  • Libby, et al., “Inflammation and Atherosclerosis,” Circulation, Journal of the American Heart Association, 105, pp. 1135-1143 (2002).
  • Lo, et al., “Paradoxical long-term proarrhythmic effects after ablating the ‘head station’ ganglionated plexi of the vagal innervation to the heart,” Heart Rhythm, vol. 10, No. 5, pp. 751-757 (May 2013).
  • Lohmeier, et al., “Prolonged Activation of the Barorelfex Produces Sustained Hypotension,” Hypertension, Journal of the American Heart Association, 43, pp. 306-311 (2004).
  • Lu, et al., “Vagal nerve stimulation protects cardiac injury by attenuating mitochondria) dysfunction in a murine burn injury model,” J. Cell. Mol. Med., vol. 17, No. 5, pp. 664-671 (2013).
  • Lw, et al., “Differing sympathetic and vagal effects on atrial fibrillation in dogs: role of refractoriness heterogeneity,”Am. J. Physiol. 273 (Heart Circ. Physiol. 42), pp. H805-H816 (1997).
  • Ma, et al., “Analysis of afferent, central, and efferent components of the baroreceptor reflex in mice,” Am J Physiol Regulatory Integration Comp Physiol, 283, pp. 1033-1040 (2002).
  • Maj, et al., “P5775: Autonomic imbalance and circulating androgens and estrogens in men with systolic heart failure,” European Heart Journal, 32 (Abstract Supplement), pp. 1090 (2011).
  • Malkin, et al., “Life-saving or life-prolonging? Interpreting trial data and survival curves for patients with congestive heart failure,” The European Journal of Heart Failure, 7, pp. 143-148 (2005).
  • Mann, “Chapter 12—Peripheral Nerves,” The Nervous System in Action, michaeldmann.net/mannl2.html, (Jul. 2011).
  • Mann, “Inflammatory Mediators and the Failing Heart. Past, Present, and the Foreseeable Future,” Circ Res., 91, pp. 988-998 (2002).
  • Mann, “Stress-Activated Cytokines and the Heart: From Adaptation to Maladaptation,” Annu. Rev. Physiol., 65, pp. 81-101 (2003).
  • Martin-Portugues, et al., “Histopathologic features of the vagus nerve after electrical stimulation in swine,” Histol Histopathol, 20, pp. 851-856 (2005).
  • Martins, et al., “Distribution of Local Repolarization Changes Produced by Efferent Vagal Stimulation in the Canine Ventricles,” JACC, vol. 2, No. 6, pp. 1191-1199 (Dec. 1983).
  • Massari, et al., “Neural control of left ventricular contractility in the dog heart: synaptic interactions of negative inotropic vagal preganglionic neurons in the nucleus ambiguus and tyrosine hydroxylase immunoreactive terminals,” Brain Research, 802, pp. 205-220 (1998).
  • May, et al., “P564: Long-term prediction of all-cause mortality in diabetic autonomic neuropathy: simple function tests or 24-hour heart rate variability (HRV)?” European Heart Journal, 32 (Abstract Supplement, pp. 64 (2011).
  • Mei, et al., “The Composition of the Vagus Nerve of the Cat,” Cell Tissue Res., 209, pp. 423-431 (1980).
  • Merrill, et al., “Electrical stimulation of excitable tissue: design of efficacious and safe protocols,” Journal of Neuroscience Methods, 141, pp. 171-198 (2005).
  • Mortara, et al., “Arterial Baroreflex Modulation of Heart Rate in Chronic Heart Failure,” Circulation, Journal of the American Heart Association, vol. 96, No. 10, pp. 3450-3458 (Nov. 18, 1997).
  • Murakawa, et al., “Effect of Cervical Vagal Nerve Stimulation on Defibrillation Energy,” Jpn Heart J, 44, pp. 91-100 (Jan. 2003).
  • Naito, “Effects of zatebradine and propranolol on canine ischemia and reperfusion-induced arrhythmias,” European Journal of Pharmacology, 388, pp. 171-176 (2000).
  • Nakajima, et al., “Autonomic Control of the Location and Rate of the Cardiac Pacemaker in the Sinoatrial Fat Pad of Parasympathetically Denervated Dog Hearts,” Journal of Cardiovascular Electrophysiology, vol. 13, No. 9 pp. 896-901 (Sep. 2002).
  • Nearing, et al., “Crescendo in Depolarization and Repolarization Heterogeneity Heralds Development of Ventricular Tachycardia in Hospitalized Patients with Decompensated Heart Failure,” Circulation Arrhythmia and Electrophysiology, Journal of the American Heart Association, 5, pp. 84-90 (2012).
  • Nihei, et al., “Decreased Vagal Control Over Heart Rate in Rats with Right-Sided Congestive Heart Failure—Downregulation of Neuronal Nitric Oxide Synthase,” Gire J, 69, pp. 493-499 (2005).
  • Ninomiya, “Direct Evidence of Nonuniform Distribution of Vagal Effects on Dog Atria,” Circulation Research, vol. XIX, pp. 576-583 (Sep. 1966).
  • Nolan, et al., “Prospective Study of Heart Rate Variability and Mortality in Chronic Heart Failure: Results of the United Kingdom Heart Failure Evaluation and Assessment of Risk Trial (UK-Heart),” Circulation, Journal of the American Heart Association, 98, pp. 1510-1516 (1998).
  • Ochoa, et al., “P2497: Effects of insulin resistance on resting heart rate, baroreflex sensitivity and indices of autonomic cardiovascular modulation in individuals with high blood pressure levels,” European Heart Journal, 32 (Abstract Supplement, pp. 431-432 (2011).
  • Ogawa, et al., “Left Stellate Ganglion and Vagal Nerve Activity and Cardiac Arrhythmias in Ambulatory Dogs with Pacing-Induced Congestive Heart Failure,” Journal of the American College of Cardiology, vol. 50, No. 4, pp. 335-444 (2007).
  • Okada, et al., “Cyclic Stretch Upregulates Production of Interleukin-8 and Monocyte Chemotactic and Activating Factor/Monocyte Chemoattractant Protein-1 in Human Endothelial Cells,” Arterioscler Thromb Vase Biol., 18, pp. 894-901 (1998).
  • Oliveira, et al., “Effects of vagal stimulation on induction and termination of atrial fibrillation in an in vivo rabbit heart model,” Rev Port Cardiol, 29(03), pp. 375-389 (2010).
  • Olshansky, et al., “Parasympathetic Nervous System and Heart Failure: Pathophysiology and Potential Implications for Therapy,” Circulation, Journal of the American Heart Association, 118, pp. 863-871 (2008).
  • Onkka, et al., “Sympathetic nerve fibers and ganglia in canine cervical vagus nerves: Localization and quantitation,” Heart Rhythm, vol. 10, No. 4, pp. 585-591 (Apr. 2013).
  • Ordelman, et al., “Selectivity for Specific Cardiovascular Effects of Vagal Nerve Stimulation with a Multi-Contact Electrode Cuff,” IEEE, pp. 1-6 (2011).
  • Packer, et al., “Effect of Carvedilol on Survival in Severe Chronic Heart Failure,” The New England Journal of Medicine, vol. 344, No. 22, pp. 1651-1658 (May 31, 2001).
  • Pavlov, et al., “Central muscarinic cholinergic regulation of the systemic inflammatory response during endotoxemia,” PNAS, vol. 103, No. 13, pp. 5219-5223 (Mar. 28, 2006).
  • Pavlov, et al., “Controlling inflammation: the cholinergic anti-inflammatory pathway,” Biochemical Society Transactions, vol. 34, part 6, pp. 1037-1040 (2006).
  • PCT Application No. PCT/US2012/068205, Search Report and Written Opinion dated Feb. 8, 2013, 15 pages.
  • PCT Application No. PCT/US2012/068211, Search Report and Written Opinion dated Jun. 13, 2013.
  • PCT Application No. PCT/US2012/068213, Search Report and Written Opinion dated Mar. 15, 2013, 11 pages.
  • PCT Application No. PCT/US2012/068223, Search Report and Written Opinion dated Apr. 3, 2013, 11 pages.
  • PCT Application No. PCT/US2013/021964, Search Report and Written Opinion dated Jul. 25, 2013, 9 pages.
  • PCT Application No. PCT/US2013/050390, Search Report and Written Opinion dated Nov. 5, 2013.
  • PCT Application No. PCT/US2013/068541, Search Report and Written Opinion dated Jan. 7, 2014.
  • PCT Application No. PCT/US2014/024827, Search Report and Written Opinion dated Nov. 11, 2014, 18 pages.
  • PCT Application No. PCT/US2015/043878, Search Report and Written Opinion dated Oct. 20, 2015, 13 pages.
  • Peckham, et al., “Chapter 18—Implantable Neural Stimulators,” Neuromodulation, Academic Press (2009).
  • Pina, et al., “The Predictive Value of Biomarkers in Heart Failure,” Medscape Education Cardiology, Available at http://www.medscape.org/viewarticle/765328 (CME Released: Jun. 15, 2012).
  • Pitzalis, et al., “Comparison Between Noninvasive Indices of Baroreceptor Sensitivity and the Phenylephrine Method in Post-Myocardial Infarction Patients,” Circulation, Journal of the American Heart Association, 97, pp. 1362-1367 (1998).
  • Poole-Wilson, “Relation of Pathophysiologic Mechanisms to Outcome in Heart Failure,” JACC, vol. 22, No. 4 (supplement A), pp. 22A-9A (Oct. 1993).
  • Pye, et al., “Study of serum C-reactive protein concentration in cardiac failure,” Br Heart J, 63, pp. 228-230 (1990).
  • Rademacher, et al., “P5878: Multidimensional halter-based analysis of cardiac autonomic regulation predicts early AF recurrence after electrical cardioversion,” European Heart Journal, 32 (Abstract Supplement), pp. 1116-1117 (2011).
  • Randall, et al., “Regional vagosympathetic control of the heart,” American Journal of Physiology, vol. 227, No. 2, pp. 444-452 (1974).
  • Randall, et al., “Selective Vagal Innervation of the Heart,” Annals of Clinical and Laboratory Science, vol. 16, No. 3, pp. 198-208 (1986).
  • Raymond, et al., “Elevated interleukin-6 levels in patients with asymptomatic left ventricular systolic dysfunction,” American Heart Journal, vol. 141, No. 3, pp. 435-438 (Mar. 2001).
  • Rhee, et al., “Effects of suprathreshold vagal stimulation on stellate ganglion nerve activity in ambulatory dogs,” 33rd Annual Scientific Sessions, Heart Rhythm, Presentation Abstract (2012).
  • Riccio, et al., “Interganglionic segregation of distinct vagal afferent fibre phenotypes in guinea-pig airways,” Journal of Physiology, 495.2, pp. 521-530 (1996).
  • Riddle, et al., “Epidemiologic Relationships Between A1C and All-Cause Mortality During a Median 3.4-Year Follow-up of Glycemic Treatment in the ACCORD Trial,” Diabetes Care, vol. 33, No. 5, pp. 983-990 (May 2010).
  • Ridker, C-Reactive Protein: A Simple Test to Help Predict Risk of Heart Attack and Stroke, Journal of the American Heart Association, 108, pp. e81-e85 (2003).
  • Ridker, et al., “Comparison of C-Reactive Protein and Low-Density Lipoprotein Cholesterol Levels in the Prediction of First cardiovascular Events,” New England Journal of Medicine, vol. 347, No. 20, pp. 1557-1566 (Nov. 14, 2002).
  • Ridker, et al., “C-Reactive Protein and Other Markers of Inflammation in the Prediction of Cardiovascular Disease in Women,” The New England Journal of Medicine, vol. 342, No. 12, pp. 836-841 (Mar. 23, 2000).
  • Ridker, et al., “Inflammation, Pravastatin, and the Risk of Coronary Events After Myocardial Infarction in Patients With Average Cholesterol Levels,” Circulation, Journal of the American Heart Association, 98, pp. 839-844 (1998).
  • Roger, et al., “Heart Disease and Stroke Statistics—2011 Update: A Report from the American Heart Association,” Circulation, Journal of the American Heart Association. Available at http://circ.ahaiournals.oro/content/123/4/e18 (2010).
  • Romanovsky, et al., “The vagus nerve in the thermoregulatory response to systemic inflammation,” Am. J. Physiol., 273, pp. R407-R413 (1997).
  • Rossi, et al., “Epicardial ganglionated plexus stimulation decreases postoperative inflammatory response in humans,” Heart Rhythm, vol. 9, No. 6, pp. 943-950 (Jun. 2012).
  • Rouse, et al., “The haemodynamic actions of ZENCA ZD7288, a novel sino-atrial node function modulator, in the exercising beagle: a comparison with zategradine and propranolol,” Abstract, British Journal of Pharmacology, 113(3):1071-7 (1994).
  • Rozman, et al., “Heart function influenced by selective mid-cervical left vagus nerve stimulation in a human case study,” Hypertension Research, 32, pp. 1041-1043 (2009).
  • Rutecki, “Anatomical, Physiological and Theoretical Basis for the Antiepileptic Effect of Vagus Nerve Stimulation,” Epilepsia, 31 (suppl. 2), pp. S1-S6 (1990).
  • Sabbah et al., “Vagus Nerve Stimulation in Experimental Heart Failure,” Heart Failure Reviews, vol. 16, No. 2, Mar. 2011, pp. 171-178.
  • Sabbah, et al., “3722: Vagus nerve stimulation improves left ventricular function in heart failure: results of a 6 month investigation with a cross-over design in dogs with experimental heart failure,” European Heart Journal, 32 (Abstract Supplement), pp. 642 (2011).
  • Sabbah, et al., “Baroreflex Activation Therapy for the Treatment of Heart Failure,” Presentation available at http://www.cvrx.com/wp/wp-contenUuploads/2012/04/Dr.-Sabbah-Slides.pdf (2012).
  • Sabbah, et al., “Chronic Electrical Stimulation of the Carotid Sinus Baroreflex Improves Left Ventricular Function and Promotes Reversal of Ventricular Remodeling in Dogs with Advanced Heart Failure,” Circulation Heart Failure, Journal of the American Heart Association, 4, pp. 65-70 (2011).
  • Samara, et al., “The Effects of Cardiac Resynchronization Therapy on Chronotropic Incompetence in Patients Intolerant of Beta Antagonist Therapy,” Journal of Cardiac Failure, vol. 17, No. 8S, pp. S54-S55 (Aug. 2011).
  • Sanner, et al., “P4743: Prediction of cardiovascular risk from nocturnal pulse wave signal using the autonomic state indicator (ASI) technology,” European Heart Journal, 32 (Abstract Supplement), pp. 839 (2011).
  • Sato, et al., “Serial Circulating Concentrations of C-Reactive Protein, Interleukin (IL)-4, and IL-6 in Patients with Acute Left Heart Decompensation,” Clin. Cardiol. 22, pp. 811-813 (1999).
  • Schauerte, “Time for Change: Cardiac neurophysiology meets cardiac electrophysiology,” Editorial Commentary, Heart Rhythm Society (2013).
  • Schiereck, et al., “AV blocking due to asynchronous vagal stimulation in rats,” Am J Physiol Heart Gire Physiol, 278, pp. H67-H73 (2000).
  • Schocken, et al., “Prevalence and Mortality Rate of Congestive Heart Failure in the United States,” JACC, vol. 20, No. 2, pp. 301-306 (Aug. 1992).
  • Schwartz, “Vagal Stimulation for Heart Diseases: From Animals to Men,” Circulation Journal, vol. 75, pp. 20-27 (Jan. 2011).
  • Schwartz, “Vagal stimulation for heart failure,” Current Opinion in Cardiology, 26, pp. 51-54 (2011).
  • Schwartz, “Vagal stimulation for the treatment of heart failure: a translational success story,” Heart, vol. 98, No. 23, pp. 1687-1690 (2012).
  • Schwartz, et al. Vagal stimulation for heart failure: Background and first in-man study, Heart Rhythm, 6, 11 suppl., pp. S76-S81 (Nov. 2009).
  • Schwartz, et al., “Long term vagal stimulation in patients with advanced heart failure. First experience in man,” European Journal of Heart Failure, 10, pp. 884-891.
  • Schwartz, et al., “Autonomic mechanisms and sudden death. New insights from analysis of baroreceptor reflexes in conscious dogs with and without myocardial infarction,” Circulation, Journal of the American Heart Association, 78, pp. 969-979 (1988).
  • Schwartz, et al., “Effects of Unilateral Cardiac Sympathetic Denervation on the Ventricular Fibrillation Threshold,” The American Journal of Cardiology, vol. 37, pp. 1034-1040 (Jun. 1976).
  • Schwartz, et al., “Sympathetic-parasympathetic interaction in health and disease: abnormalities and relevance in heart failure,” Heart Fail Rev, 16, pp. 101-107 (2011).
  • Seta, et al., “Basic Mechanisms in Heart Failure: The Cytokine Hypothesis,” Journal of Cardiac Failure, vol. 2, No. 3, pp. 243-249 (1996).
  • Sha, et al., “Low-Level Right Vagal Stimulation: Anticholinergic and Antiadrenergic Effects,” J Cardiovasc Electrophysiol, pp. 1-7 (Feb. 2011).
  • Shamoon, et al., The Diabetes Control and Complications Trial Research Group, “The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent Diabetes mellitus,” The New England Journal of Medicine, vol. 329, No. 14, pp. 977-986 (Sep. 30, 1993).
  • Shannon, “A Model of Safe Levels for Electrical Stimulation,” IEEE Transactions on Biomedical Engineering, vol. 39, No. 4, pp. 424-426 (Apr. 1992).
  • Shen, et al., “Continuous Low-Level Vagus Nerve Stimulation Reduces Stellate Ganglion Nerve Activity and Paroxysmal Atrial Tachyarrhythmias in Ambulatory Canines,” Circulation, Journal of the American Heart Association, 123, pp. 2204-2212 (2011).
  • Shen, et al., “Low-level vagus nerve stimulation upregulates small conductance calcium-activated potassium channels in the stellate ganglion,” Heart Rhythm, vol. 10, No. 6, pp. 910-915 (2013).
  • Shinohara, et al., “Heart Failure Decreases Nerve Activity in the Right Atrial Ganglionated Plexus,” J Cardiovasc Electrophysiol, pp. 1-9 (2011).
  • Shioi, et al., “Increased Expression of Interleukin-1B and Monocyte Chemotactic and Activating Factor/Monocyte Chemoattractant Protein-1 in the Hypertrophied and Failing Heart with Pressure Overload,” Gire Res., 81, pp. 664-671 (1997).
  • Singal, et al., “The role of oxidative stress in the genesis of heart disease,” Cardiovascular Research, 40, pp. 426-432 (1998).
  • Spuck, et al., “Right-sided vagus nerve stimulation in humans: An effective therapy?” Epilepsy Research, pp. 1-3 (2008).
  • Stein, et al., “A Simple Method to Identify Sleep Apnea Using Hotter Recordings,” J Cardiovasc Electrophysiol, vol. 14, pp. 467-473 (May 2003).
  • Stein, et al., “Feasibility of Using Mobile Cardiac Outpatient Telemetry (MCOT) to Identify Severe Sleep Disorders” (2009).
  • Stieber, et al., “Bradycardic and proarrhythmic properties of sinus node inhibitors,” Abstract, Molecular Pharmacology, 69(4):1328-37 (2006).
  • Taylor, et al., “The unequal influences of the left and right vagi on the control of the heart and pulmonary artery in the rattlesnake, Grata/us durissus,” The Journal of Experimental Biology, 212, pp. 145-151 (2009).
  • Thayer, et al., “The role of vagal function in the risk for cardiovascular disease and mortality,” Biological Psychology, 74, pp. 224-242 (2007).
  • Thollon, et al., “Electrophysiological effects of S 16257, a novel sino-atrial node modulator, on rabbit and guinea-pig cardiac preparations: comparison with UL-FS 49,” Abstract, British Journal of Pharmacology, 112(1):37-42 (1994).
  • Tosato, et al., “Quasi-trapezoidal pulses to selectively block the activation of intrinsic laryngeal muscles during vagal nerve stimulation,” J. Neural Eng., 4, pp. 205-212 (2007).
  • Tsutsumi, et al., “Modulation of the myocardial redox state by vagal nerve stimulation after experimental myocardial infarction,” Cardiovascular Research, 77, pp. 713-721 (2008).
  • Tyler, et al., “Chapter 17—Electrodes for the Neural Interface,” Neuromodulation, Academic Press (2009).
  • Ulphani, et al., “Quantitative analysis of parasympathetic innervation of the porcine heart,” Heart Rhythm, 7, pp. 1113-1119 (2010).
  • Uthman, et al., “Effectiveness of vagus nerve stimulation in epilepsy patients. A 12-year observation,” Neurology, 63, pp. 1124-1126 (2004).
  • Van Stee, “Autonomic Innervation of the Heart,” Environmental Health Perspectives, vol. 26, pp. 151-158 (1978).
  • Vanoli, et al., “Vagal stimulation and prevention of sudden death in conscious dogs with a healed myocardial infarction,” Circulation Research, Journal of the American Heart Association, 68, pp. 1471-1481 (1991).
  • Vasan, et al., “Inflammatory Markers and Risk of Heart Failure in Elderly Subjects Without Prior Myocardial Infarction,” Circulation, Journal of the American Heart Association, 107, pp. 1486-1491 (2003).
  • Vassalle, et al., “An Analysis of Arrhythmias Induced by Ouabain in Intact Dogs,” Circulation Research, Journal of the American Heart Association, 13, pp. 132-148 (1963).
  • Velagaleti, et al., “Long-Term Trends in the Incidence of heart Failure After Myocardial Infarction,” 118, pp. 2057-2062 (2008).
  • Verrier, et al., “Microvolt T-Wave Alternans,” Journal of the American College of Cardiology, vol. 58, No. 13, pp. 1309-1324 (2011).
  • Vimercati, et al., “Acute vagal stimulation attenuates cardiac metabolic response to B-adrenergic stress,” The Journal of Physiology, vol. 500, No. 23, pp. 6065-6074 (2012).
  • Wang, et al., “Nicotinic acetylcholine receptor alpha-7 subunit is an essential regulator of inflammation,” Nature, vol. 421, pp. 384-388 (Jan. 23, 2003).
  • Wang, et al., “Synaptic and Neurotransmitter Activation of Cardiac Vagal Neurons in the Nucleus Ambiguus,” Annals New York Academy of Sciences, pp. 237-246 (2001).
  • Waninger, et al., “Characterization of Atrioventricular Nodal Response to Electrical Left Vagal Stimulation,” Annals of Biomedical Engineering, vol. 27, pp. 758-762 (1999).
  • Wann, “Behavioural signs of depression and apoptosis in the limbic system following myocardial infarction: effects of sertraline,” Journal of Psychopharmacology, 23(4), pp. 451-459 (2009).
  • Wann, et al., “Vulnerability for apoptosis in the limbic system after myocardial infarction in rats: a possible model for human postinfarct major depression,” J Psychiatry Neurosci, 32(1):11-6, pp. 11-16 (2007).
  • Watkins, et al., “Cytokine-to-Brain Communication: A Review & Analysis of Alternative Mechanisms,” Life Sciences, vol. 57, No. 11, pp. 1011-1026 (1995).
  • Whyte, et al., “Reactive oxygen species modulate neuronal excitability in rat intrinsic cardiac ganglia,” Auton Neurosci, 150(1-2), pp. 45-52 (Oct. 5, 2009).
  • Yang, et al., “Sustained increases in heart rate induced by time repetition of vagal stimulation in dogs,” Am. J. Physiol., 249, pp. H703-H709 (1985).
  • Yin, et al., “Independent prognostic value of elevated high-sensitivity C-reactive protein in chronic heart failure,” American Heart Journal, vol. 147, No. 5, pp. 931-938 (2004).
  • Yndestad, et al., “Systemic inflammation in heart failure—The whys and wherefores,” Heart Fail Rev, 11, pp. 83-92 (2006).
  • Yoo, et al., “High-resolution measurement of electrically-evoked vagus nerve activity in the anesthetized dog,” J. Neural Eng., 10, pp. 1-9 (2013).
  • Yoo, et al., “Selective Control of Physiological Responses by Temporally-Patterned Electrical Stimulation of the Canine Vagus Nerve,” 33rd Annual International Conference of the IEEE EMBS (2011).
  • Yu, et al., “Interactions between atrial electrical remodeling and autonomic remodeling: How to break the vicious cycle,” Heart Rhythm, 9, pp. 804-809 (2012).
  • Yu, et al., “Low-level transcutaneous electrical stimulation of the auricular branch of the vagus nerve: A noninvasive approach to treat the initial phase of atrial fibrillation,” Heart Rhythm, 10, pp. 428-435 (2013).
  • Yuan, et al., “Gross and Microscopic Anatomy of the Canine Intrinsic Cardiac Nervous System,” The Anatomical Record, 239, pp. 75-87 (1994).
  • Yusuf, et al., “Changes in Hypertension Treatment and in Congestive Heart Failure Mortality in the United States,” Hypertension, Journal of the American Heart Association, 13:174-1179 (1989).
  • Zhang, et al., “Arrhythmias and vagus nerve stimulation,” Heart Fail Rev, 16, pp. 147-161 (2011).
  • Zhang, et al., “Involvement of activated astrocyte and microglia of locus coeruleus in cardiac pain processing after acute cardiac injury,” Neurol Res, 31, pp. 432-438 (2009).
  • Zhang, et al., “Relationship between right cervical vagus nerve stimulation and atrial fibrillation inducibility: Therapeutic intensities do not increase arrhythmogenesis,” Heart Rhythm, 6, pp. 244-250 (2009).
  • Zhang, et al., “Therapeutic Effects of Selective Atrioventricular Node Vagal Stimulation in Atrial Fibrillation and Heart Failure,” Journal of Cardiovascular Electrophysiology, vol. 24, Issue 1, pp. 86-91 (2012).
  • Zheng, et al., “Vagal stimulation markedly suppresses arrhythmias in conscious rats with chronic heart failure after myocardial infarction,” Proceedings of the 2005 IEEE (2005).
  • Zipes, et al., “Effects of selective vagal and stellate ganglion stimulation on atrial refractoriness,” Cardiovascular Research, 8, pp. 647-655 (1974).
  • Zucker, et al., “Chronic Baroreceptor Activation Enhances Survival in Dogs with Pacing-Induced Heart Failure,” Journal of the American Heart Association, Hypertension (2007).
Patent History
Patent number: 10220212
Type: Grant
Filed: Dec 30, 2016
Date of Patent: Mar 5, 2019
Patent Publication Number: 20170106194
Assignee: LivaNova USA, Inc. (Houston, TX)
Inventors: Imad Libbus (St. Paul, MN), Bruce H. Kenknight (Maple Grove, MN), Badri Amurthur (Los Gatos, CA)
Primary Examiner: Eric D. Bertram
Application Number: 15/395,872
Classifications
Current U.S. Class: Hypertension Treating (607/44)
International Classification: A61N 1/36 (20060101); A61B 5/00 (20060101); A61B 5/0245 (20060101); A61B 5/0205 (20060101);